The Recall Desk

Archive

October 2015 recalls

479 recalls were announced in October 2015.

What the numbers show

Critical
22
Severe
124
High
217
Moderate
88
Low
28

Of the 479 recalls this month scored against our rubric, 5% are Critical, 26% are Severe.

Which agencies issued them

301–400 of 479

  • HighFDA (Devices)·Z-0071-2016·2015-10-14

    Resource Optimization & Innovation Recalls 158 Sterile Titanium Rib Surgical Kits

    Resource Optimization & Innovation LLC is recalling 158 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800568, Sterile, OR0658 - Titanium Rib - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0083-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Total Hip Surgical Kits

    Resource Optimization & Innovation LLC is recalling 24 sterile total hip surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 880330, Sterile, OR0761 - Total Hip - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0113-2016·2015-10-14

    Olympus MAJ-1606 Instrument Channel Adaptors Recalled for Sterility Breach

    Olympus is recalling MAJ-1606 Instrument Channel Adaptors due to small puncture marks in sterile packaging that may compromise sterility.

    Product
    MAJ-1606 Instrument Channel Adaptor; a single use adapter which enables a connection between the endoscope's instrument channel port and the O FP-2 pump's tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0034-2016·2015-10-14

    FDA Recalls Sterile Neuro Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 904 sterile neuro surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800411, Sterile, NU0480 - Neuro Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pro
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0073-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 24 sterile surgical kits because a component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800597, Sterile, GY0688 - LAVH - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedu
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0090-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Open Heart Surgical Kits

    Resource Optimization & Innovation LLC is recalling 440 sterile open heart surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800410001, Sterile, CV0479A - Open Heart Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a sur
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0088-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Orthopedic Surgical Kits

    Resource Optimization & Innovation LLC is recalling 1,476 sterile orthopedic surgical kits because the equipment glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800407001, Sterile, OR0476A - Ortho Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0054-2016·2015-10-14

    Resource Optimization & Innovation LLC Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 144 sterile C-section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800535, Sterile, LD0620 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0108-2016·2015-10-14

    Beckman Coulter Recalls MICroSTREP plus 1 and 2 Panels for Manufacturing Error

    Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation and false resistant results.

    Product
    MICroSTREP plus 1 Panel, Part No. B1027-201 Product Usage: MicroScan MICroSTREP plus panels are designed for use in determining quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including Streptococcus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0066-2016·2015-10-14

    FDA Recalls 448 Sterile Laparoscopic Cholecystectomy Surgical Kits

    Resource Optimization & Innovation LLC is recalling 448 sterile surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800560, Sterile, GS0649 - Lap Chole - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0051-2016·2015-10-14

    FDA Recalls 48 Neuro Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 48 sterile neuro surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800531, Sterile, NU0615 - Neuro Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pro
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0100-2016·2015-10-14

    FDA Recalls Pediatric Heart Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 57 pediatric heart surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number 800565001, Sterile, CV0654A - Pediatric Heart - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a su
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0049-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Hip Shoulder Surgical Kits

    Resource Optimization & Innovation LLC is recalling 92 sterile hip shoulder surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800527, Sterile, OR0611 - Hip Shoulder Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0056-2016·2015-10-14

    Resource Optimization & Innovation LLC Recalls Sterile Extremity Surgical Kits

    Resource Optimization & Innovation LLC is recalling 672 sterile extremity surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800548, Sterile, OR0637 - Extremity - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0099-2016·2015-10-14

    FDA Recalls 88 Sterile Lap Chole Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 88 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800560001, Sterile, GS0649A - Lap Chole - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0094-2016·2015-10-14

    Resource Optimization & Innovation Recalls 164 Arthroscopy Surgical Kits

    Resource Optimization & Innovation LLC is recalling 164 arthroscopy surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800422001, Sterile, OR0491A - Arthroscopy Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a sur
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0096-2016·2015-10-14

    FDA Recalls 924 Sterile Lap Chole Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 924 sterile surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800528001, Sterile, GS0612A - Lap Chole Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighNHTSA·15V657000·2015-10-14

    Mercedes-Benz Recalls 2015 S-Class Models Due to Seat Belt Installation Error

    Mercedes-Benz is recalling 2,580 model year 2015 S550 4Matic, AMG S63, and AMG S65 vehicles because front seat belts may be installed on the wrong side, affecting crash protection.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S63, AMG S65, S550 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V656000·2015-10-14

    Toyota Recalls 2016 Tacoma Trucks Due to Knee Air Bag Bolt Issue

    Toyota is recalling 2016 Tacoma trucks because incorrect bolts were used to install the driver's knee air bag module, which may loosen over time.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0036-2016·2015-10-14

    Resource Optimization & Innovation Recalls 874 Sterile Surgical Kits

    Resource Optimization & Innovation LLC is recalling 874 sterile surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800414, Sterile, OR0483 - Total Joint Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0032-2016·2015-10-14

    FDA Recalls Sterile Surgical Kits Due to Potential Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 3,099 sterile surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800409, Sterile, GS0478 - LAP Chole Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgica
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0026-2016·2015-10-14

    Ortho Solutions Recalls UltOS 3.5mm Locking Screws Due to Manufacturing Defect

    Ortho Solutions Inc is recalling 875 units of UltOS 3.5mm locking screws because the locking thread feature was not manufactured to specification, creating a risk that the screw may not lock onto the plate.

    Product
    Ortho OS Solutions UltOS 3.5mm locking screw 12mm to 50mm Ortho Solutions LTD, Unit 5 West Station Business Park, Spital Road, Maldon, Essex CM96FF Rx Only a) Sterile b) Non-Sterile Orthopaedic Bone Screw
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0042-2016·2015-10-14

    Resource Optimization & Innovation Recalls 124 Sterile Arthroscopy Surgical Kits

    Resource Optimization & Innovation LLC is recalling 124 sterile arthroscopy surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800422, Sterile, OR0491 - Arthroscopy Pk - surgical kit containing cover light handle soft, Rx. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0031-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 600 sterile C-section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800408, Sterile, LD0477 - C-Section Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROI, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0030-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Orthopedic Surgical Kits

    Resource Optimization & Innovation LLC is recalling 1,476 sterile orthopedic surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800407, Sterile, OR0476 - Ortho Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROI, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0098-2016·2015-10-14

    Resource Optimization & Innovation Recalls Pediatric Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 158 pediatric surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800554002, Sterile, GS0643B - Pediatric Basic - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a su
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0037-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Shoulder Surgical Kits

    Resource Optimization & Innovation LLC is recalling 832 sterile shoulder surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800415, Sterile, OR0484 - Shoulder System Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a s
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0081-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Open Heart Surgical Kits

    Resource Optimization & Innovation LLC is recalling 54 sterile open heart surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 880327, Sterile, CV0758 - Open Heart A&B - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surg
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0072-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Open Heart Surgical Kits

    Resource Optimization & Innovation LLC is recalling 108 sterile open heart surgical kits because an equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800569, Sterile, CV0659 - Open Heart A & B - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surg
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0095-2016·2015-10-14

    FDA Recalls 230 Sterile C-Section Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 230 sterile C-section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800524001, Sterile, LD0608A - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0048-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Head and Neck Surgical Kits

    Resource Optimization & Innovation LLC is recalling 156 sterile surgical kits because a component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800526, Sterile, ET0610 - Head and Neck - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgica
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0044-2016·2015-10-14

    FDA Recalls 146 Sterile C-Section Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 146 sterile C-section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800508, Sterile, LD0586 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical p
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0076-2016·2015-10-14

    FDA Recalls 164 Neuro Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 164 sterile neuro surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800617, Sterile, NU0768 - Neuro Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pro
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0038-2016·2015-10-14

    FDA Recalls Robotic Hysterectomy Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 324 robotic hysterectomy surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800416, Sterile, GY0485 - Robotic Hysterectomy Pkg - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use duri
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0104-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Open Heart Surgical Kits

    Resource Optimization & Innovation LLC is recalling 36 sterile Open Heart surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 880327002, sterile, CV0758B - Open Heart A&B - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a s
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0097-2016·2015-10-14

    Resource Optimization & Innovation LLC Recalls Pediatric Surgical Kits

    Resource Optimization & Innovation LLC is recalling 136 sterile pediatric surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800554001, Sterile, GS0643A - Pediatric Basic - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a su
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0102-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Titanium Rib Surgical Kits

    Resource Optimization & Innovation LLC is recalling 62 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number 800568001, Sterile, OR0658A - Titanium Rib - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0041-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Surgical Kits Due to Sterility Risk

    Resource Optimization & Innovation LLC is recalling 1,220 sterile surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800419, Sterile, GY0488 - D&C Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical proc
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0029-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Surgical Kits Due to Sterility Risk

    Resource Optimization & Innovation LLC is recalling 7,904 sterile surgical kits because the equipment glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800401, Sterile, GS0470 - Lap Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical proc
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0028-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 26 sterile C-section surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800091, Sterile, LD0692 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pr
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0058-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Hip Shoulder Surgical Kits

    Resource Optimization & Innovation LLC is recalling 125 sterile hip shoulder surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800550, Sterile, OR0639 - Hip Shoulder - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0039-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Laparoscopy Surgical Kits

    Resource Optimization & Innovation LLC is recalling 400 sterile laparoscopy surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800417, Sterile, GY0486 - Laparoscopy Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0080-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 1,233 sterile surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 880326, Sterile, GS0757 - Major Basin - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0084-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Total Knee Surgical Kits

    Resource Optimization & Innovation LLC is recalling 40 sterile total knee surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 880331, Sterile, OR0762 - Total Knee - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical p
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0069-2016·2015-10-14

    FDA Recalls VP Shunt Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 200 VP Shunt surgical kits because equipment gloves may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800566, Sterile, NU0655 - VP Shunt - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical pro
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0107-2016·2015-10-14

    Siemens SOMATOM Force CT Systems Recalled for Software and Firmware Bugs

    Siemens Medical Solutions USA is recalling 21 SOMATOM Force computed tomography systems due to software and firmware bugs.

    Product
    SOMATOM Force; computed tomography x-ray system. Intended to generate and process cross-sectional images of patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0046-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 144 sterile C-section surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800524, Sterile, LD0608 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical p
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0086-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 388 sterile C Section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800036003, Sterile, LD0274C - C Section Pack - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a sur
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0050-2016·2015-10-14

    Resource Optimization & Innovation Recalls 516 Sterile Lap Chole Surgical Kits

    Resource Optimization & Innovation LLC is recalling 516 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800528, Sterile, GS0612 - Lap Chole Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgica
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0093-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Vascular Surgical Kits

    Resource Optimization & Innovation LLC is recalling 500 sterile vascular surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800413001, Sterile, CV0482A - Vascular Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0091-2016·2015-10-14

    FDA Recalls 510 Sterile Neuro Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 510 sterile neuro surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800411001, Sterile, NU0480A - Neuro Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighNHTSA·15V655000·2015-10-14

    Mercedes-Benz Recalls 2014-2015 B-Class Electric Drive Vehicles for Software Defect

    Mercedes-Benz is recalling 2,618 model year 2014-2015 B-Class Electric Drive vehicles because a communication error may cause the electric powertrain to shut down, temporarily immobilizing the vehicle.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ B-CLASS ELECTRIC, B 250E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0005-2016·2015-10-14

    Caribou Coffee Recalls Biscotti for Missing Soy Ingredient Labeling

    Caribou Coffee Company Inc. is recalling two types of biscotti because soy lecithin was missing from the ingredient list.

    Product
    Caribou Chocolate Chip Toffee Pecan Biscotti, Net Wt. 1.4 oz. (40g) in clear cello flow wrap bag.
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-0001-2016·2015-10-14

    General Mills Recalls Cascadian Farm Frozen Cut Green Beans

    General Mills is recalling a limited quantity of frozen Cascadian Farm Cut Green Beans after one package tested positive for Listeria monocytogenes.

    Product
    Cascadian Farm Organic Cut Green Beans, Net. Wt. 16 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 1,400 sterile C-section surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800408001, Sterile, LD0477A - C-Section Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surg
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0079-2016·2015-10-14

    Resource Optimization & Innovation LLC Recalls Sterile C-Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 72 sterile C-section surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 880323, Sterile, LD0754 - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical p
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0061-2016·2015-10-14

    FDA Recalls Pediatric Surgical Kits Due to Potential Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 746 sterile pediatric surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800554, Sterile, GS0643 - Pediatric Basic - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgi
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0060-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Total Knee Surgical Kits

    Resource Optimization & Innovation LLC is recalling 200 sterile total knee surgical kits because the equipment glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800553, Sterile, OR0642 - Total Knee - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical p
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0085-2016·2015-10-14

    FDA Recalls 658 Sterile Surgical Kits Due to Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 658 sterile surgical kits because equipment glove components may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800036002, Sterile, LD0274B - C Section Pack - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a sur
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0114-2016·2015-10-14

    Stryker Recalls Disposable Paper Filters for Sterilization Containers

    Stryker is recalling disposable paper filters for sterilization containers because inhomogeneous paper may compromise the sterile barrier during shelf-life.

    Product
    Disposable Paper Filter for Sterilization Containers Paper, Medical Accessory, 100 DISP, Paper F, Steri.Cases, New Shape, Manufactured and distributed by Stryker Leibinger GmbH & Co KG, Distributed in the USA by: Stryker Orthopedics, NON STERILE.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0057-2016·2015-10-14

    FDA Recalls 114 Sterile Head and Neck Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 114 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800549, Sterile, ET0638 - Head & Neck - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0045-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile C Section Surgical Kits

    Resource Optimization & Innovation LLC is recalling 222 sterile C Section surgical kits because the equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800514, Sterile, LD0592 - C Section Pack - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROI, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgic
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0077-2016·2015-10-14

    FDA Recalls 100 Neurosurgical Kits Due to Potential Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 100 sterile neurosurgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800623, Sterile, NU0787 - Neuro - surgical kit containing light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical procedure
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0087-2016·2015-10-14

    Resource Optimization & Innovation Recalls Sterile Surgical Kits Due to Sterility Concerns

    Resource Optimization & Innovation LLC is recalling 68 sterile surgical kits because equipment glove components may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800091001, Sterile, LD0692A - C Section - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a surgical
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0103-2016·2015-10-14

    Resource Optimization & Innovation Recalls 37 Sterile Open Heart Surgical Kits

    Resource Optimization & Innovation LLC is recalling 37 sterile open heart surgical kits because a glove component may have splits or holes that compromise sterility.

    Product
    regard Item Number: 800569001, Sterile, CV0659A - Open Heart A&B - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a su
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0040-2016·2015-10-14

    FDA Recalls Sterile Surgical Kits Due to Potential Sterility Compromise

    Resource Optimization & Innovation LLC is recalling 296 sterile surgical kits because an equipment glove component may contain splits or holes that compromise sterility.

    Product
    regard Item Number: 800418, Sterile, GY0487 - Major Vaginal Pk - surgical kit containing cover light handle soft, RX. The responsible firm on the label is ROi, LLC, St. Louis, MO. Custom procedure tray contains surgical instruments and accessories intended for use during a sur
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0022-2016·2015-10-14

    Medtronic SureScan Pacemaker ID Cards Mislabel MR Conditional Status

    Medtronic is recalling 777 identification cards for SureScan pacemaker patients that incorrectly indicate the entire system is MR Conditional.

    Product
    Medtronic Medical Device Identification Card for SureScan pacemaker patients. The front of this card identifies the implanted pacing system components currently registered to the patient. The back of the card lists patient's following physician as well as specific messa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0027-2016·2015-10-14

    Zimmer Universal Locking System Recalled for Incorrect Silk Screening

    Zimmer, Inc. is recalling 18 units of the Universal Locking System due to incorrect catalog numbers printed on the trays.

    Product
    Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unu
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0019-2016·2015-10-14

    Siemens SOMATOM Definition Edge CT Scanner Software Recall

    Siemens Medical Solutions is recalling 113 SOMATOM Definition Edge CT scanners due to a software bug affecting visual warnings and image quality.

    Product
    SOMATOM Definition Edge; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0024-2016·2015-10-14

    Synthes Periarticular Insertion Handles and Aiming Arms Recalled for Fit Issues

    Synthes (USA) Products LLC is recalling 172 units of Periarticular Insertion Handles and Aiming Arms because they cannot be secured to subsequent device versions as intended.

    Product
    Synthes Periarticular Insertion Handle for 4.5mm LCP Proximal Tibia Plates and Periarticular Aiming Arm for 4.5mm LCP Proximal Tibia Plates
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0106-2016·2015-10-14

    Siemens Syngo RT Oncologist software update addresses safety issues

    Siemens Medical Solutions is updating Syngo RT Oncologist software versions 4.2 and 4.3 to fix safety and performance issues.

    Product
    Syngo RT Oncologist, an optional accessory to the linear accelerator system and permits localization, contouring, segmentation, image review, and review and approval of treatment plan parameters. In addition, it includes tools and administrative functions to aid in the diagnosis,
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0023-2016·2015-10-14

    GE Healthcare Recalls Centricity PACS IW Due to Missing Images

    GE Healthcare is recalling 921 Centricity PACS IW systems worldwide because images may be missing when a specific system parameter is set to a value greater than 1.

    Product
    Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and displayed within the system or across computer networks
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0105-2016·2015-10-14

    CooperSurgical LEEP REDIKIT Recalled for Incorrect Lidocaine Concentration Labeling

    CooperSurgical is recalling LEEP REDIKIT surgical kits because the labels list 2% Lidocaine HCl, but the kits contain 1% Lidocaine HCl vials.

    Product
    CooperSurgical LEEP REDIKIT-Used as a surgical preparatory kit for Loop Electrosurgical Excision Procedure P/N 6061
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-0021-2016·2015-10-14

    Siemens SOMATOM Definition AS CT Scanner Software Recall

    Siemens Medical Solutions is recalling 113 SOMATOM Definition AS CT scanners to fix a software bug affecting visual warnings and image quality.

    Product
    SOMATOM Definition AS, intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0025-2016·2015-10-14

    Integra Recalls Universal Compact Head Ring Adapter Plate Due to Assembly Error

    Integra LifeSciences Corp. is recalling six Universal Compact Head Ring Adapter Plates that do not assemble properly due to a manufacturing drawing error.

    Product
    Universal Compact Head Ring Adapter Plate (UCHRAP), a component of the Universal Compact Head Ring Adapter, UCHRA. The UCHRA is a component of the Integra¿ CRW¿ Precision Arc Stereotactic System.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0110-2016·2015-10-14

    Beckman Coulter Recalls Access Free T3 Reagent Kits Due to Filling Errors

    Beckman Coulter is recalling Access Free T3 Reagent Kits because they were filled incorrectly and contain insufficient reagents.

    Product
    Access Free T3 Reagent Kit, P/N A13422 The Access Free T3 assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of free triiodothyronine levels in human serum and plasma using the Access Immunoassay Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0109-2016·2015-10-14

    Beckman Coulter Recalls MICroSTREP plus Panels Due to Manufacturing Error

    Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation, leading to false resistant results.

    Product
    MICroSTREP plus 2 Panel, Part No. B1027-202 Product Usage: MicroScan MICroSTREP plus panels are designed for use in determining quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including Streptococcus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0003-2016·2015-10-14

    Organic Girl Baby Spinach Recalled for Elevated Cadmium Levels

    NewStar Fresh Foods is recalling Organic Girl baby spinach due to elevated cadmium levels. The product was distributed in 12 states.

    Product
    organic girl - good clean greens baby spinach - tender nutrition baby leaves. Washed 3 times. USDA Organic. 5 oz.. plastic clamshell. Distributed by organic girl, Salinas, CA 93901
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-0008-2016·2015-10-14

    Daytrana Methylphenidate Patches Recalled for Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) 30 mg patches due to a defective delivery system that failed mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0005-2016·2015-10-14

    Toshiba Recalls Celesteion PET/CT Systems Due to Data Loss Risk

    Toshiba American Medical Systems is recalling one Celesteion PCA-9000A/2 PET/CT System in Nevada because a software defect may prevent raw data from being saved during specific scans.

    Product
    Celesteion PCA-9000A/2 PET/CT System
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0020-2016·2015-10-14

    Siemens SOMATOM Definition Flash CT Scanner Software Recall

    Siemens Medical Solutions USA is recalling 113 SOMATOM Definition Flash CT scanners due to a software bug in version VA48A_SP0 that affects visual warnings and image quality.

    Product
    SOMATOM Definition Flash; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0004-2016·2015-10-14

    Blue Plate Light Mayonnaise Recalled for Incorrect Labeling

    Reily Foods Co. is recalling one lot of Blue Plate Light Mayonnaise because the packaging displays the ingredient and nutrition information for regular Blue Plate Mayonnaise.

    Product
    Blue Plate(R) LIGHT MAYONNAISE, 18 Fl OZ (1 PT 2 OZ) 532, mL. UPC 47900-50638
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·15V642000·2015-10-13

    Newmar Recalls 2016 Motorhomes Due to Parking Brake Calibration Defect

    Newmar is recalling 86 model year 2016 Bay Star and Canyon Star motorhomes because the parking brake may fail to hold the vehicle or disengage properly.

    Product
    NEWMAR — NEWMAR CANYON STAR, BAY STAR, BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V646000·2015-10-13

    E-One Emergency Vehicles Recalled for Disconnected Air Bag Harness

    E-One is recalling 2014-2015 Cyclone II, Typhoon, and Quest emergency vehicles because the front air bag harness may be disconnected, preventing deployment in a crash.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, QUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V651000·2015-10-13

    Volvo Recalls 2009-2015 VN Trucks for Steering Loss Risk

    Volvo is recalling 2009-2015 VN trucks because corrosion of ball joints may cause loss of steering. Owners should contact dealers for free inspection and replacement.

    Product
    VOLVO — VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V649000·2015-10-13

    Great Dane Recalls 2016 Trailers Due to Axle Nut Retaining Clip Defect

    Great Dane is recalling 2016 Dry Freight and Converter Dolly trailers because axle nut retaining clips may be missing or improperly seated, risking wheel loss and loss of vehicle control.

    Product
    GREAT DANE — GREAT DANE CONVERTER DOLLY, DRY FREIGHT SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V645000·2015-10-13

    Forest River Recalls 2015-2016 Trailers for Incorrect Tire Placard

    Forest River is recalling specific 2015 Wildwood and 2016 Salem recreational trailers because the tire and wheel placard lists incorrect sizes, which could lead to vehicle instability if the wrong tires are installed.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V650000·2015-10-13

    Forest River Cherokee Recalled for Incorrect Federal Placard Information

    Forest River is recalling 2013-2014 Cherokee trailers because the Federal placard displays incorrect tire and weight information, which could lead to vehicle overload.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V641000·2015-10-09

    Paccar Recalls Peterbilt and Kenworth Trucks Due to Fifth Wheel Defect

    Paccar is recalling specific 2011-2013 Peterbilt and Kenworth trucks because the fifth wheel locking mechanism may fail, potentially causing the trailer to detach.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T700, 587
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V640000·2015-10-09

    GM Recalls 2014-2015 Trucks for Ignition Lock Actuator Binding Defect

    General Motors is recalling specific 2014-2015 Chevrolet and GMC trucks because the ignition lock actuator may bind, potentially causing loss of steering and braking power.

    Product
    GMC — GMC, CHEVROLET SIERRA, SUBURBAN, SILVERADO, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V639000·2015-10-09

    PACCAR Recalls 2016 Peterbilt and Kenworth Trucks for Transmission Defect

    PACCAR is recalling 2016 Peterbilt and Kenworth trucks because the transmission may lock or cause unexpected backward movement, increasing crash risk.

    Product
    PETERBILT — PETERBILT, KENWORTH 367, 384, 579, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V638000·2015-10-09

    Starcraft RV Recalls 2016 Autumn Ridge Travel Trailers for Frame Defect

    Starcraft RV is recalling 35 model year 2016 Autumn Ridge travel trailers due to an incorrectly built frame that may cause tire failure and increase crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AUTUMN RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V637000·2015-10-09

    Ducati Recalls Multistrada Motorcycles Due to Side-Stand Defect

    Ducati is recalling 2015-2016 Multistrada 1200 and 1200 S motorcycles because the side-stand may break, causing the bike to fall over and increasing injury risk.

    Product
    DUCATI — DUCATI MULTISTRADA 1200S, MULTISTRADA 1200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V636000·2015-10-09

    GM Recalls 2014 Chevrolet Caprice and SS for Airbag Deployment Risk

    General Motors is recalling 2014 Chevrolet Caprice and SS vehicles because a missing seat bracket may cause airbags to deploy with excessive force.

    Product
    CHEVROLET — CHEVROLET CAPRICE, CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide

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