The Recall Desk

Archive

April 2017 recalls

850 recalls were announced in April 2017.

What the numbers show

Critical
99
Severe
150
High
458
Moderate
121
Low
22

Of the 850 recalls this month scored against our rubric, 12% are Critical, 18% are Severe.

Which agencies issued them

501–600 of 850

  • ModerateFDA (Drugs)·D-0627-2017·2017-04-12

    Alvogen Recalls Nifedipine Extended-Release Tablets Due to Sorafenib Cross-Contamination

    Alvogen, Inc. is recalling Nifedipine Extended-Release Tablets, 30 mg, due to cross-contamination with sorafenib powder found in the manufacturing facility's inlet air duct.

    Product
    Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1710-2017·2017-04-12

    Beckman Coulter Recalls Access 2 Immunoassay Systems Due to Circuit Board Defect

    Beckman Coulter is recalling Access 2 Immunoassay Systems because a defective circuit board can cause the device to stop running and cancel tests.

    Product
    Access 2 assay Immunoassay System, Remanufactured, Part No. 386220 Product Usage: The Access 2 and UniCel DxI Access Immunoassay Systems are in vitro diagnostic devices used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1726-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpreted instructions may cause tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Portuguese SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0650-2017·2017-04-12

    Lupin Recalls Quinapril Tablets Due to Impurity A Specification Failure

    Lupin Pharmaceuticals is recalling Quinapril 5 mg tablets because they failed impurity specifications. The recall covers 15,168 bottles distributed nationwide.

    Product
    QUINAPRIL — QUINAPRIL (QUINAPRIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1706-2017·2017-04-12

    Philips Recalls Mobile Diagnostic X-Ray Systems Due to Marker Placement Error

    Philips Healthcare Inc. is recalling 220 Mobile Diagnostic X-Ray Systems because electronic markers may be placed at the wrong anatomical position when images are moved between views.

    Product
    Mobile Diagnostic X-Ray System with Digital Panel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0631-2017·2017-04-12

    Alvogen Recalls Nifedipine Tablets Due to Sorafenib Cross-Contamination

    Alvogen Inc. is recalling Nifedipine Extended-Release Tablets, 90 mg, due to cross-contamination with sorafenib powder found in the inlet air duct.

    Product
    Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2017·2017-04-12

    Arrow International Recalls PIC Catheters Due to Labeling Error

    Arrow International is recalling 1,351 CG+ Arrow PIC Catheters due to a labeling error where lidstock and banner card codes do not match.

    Product
    The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0629-2017·2017-04-12

    Adalat CC Tablets Recalled for Sorafenib Cross-Contamination

    Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets due to cross-contamination with sorafenib powder found in the manufacturing facility.

    Product
    Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1722-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Greek SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1727-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits Due to Instruction Card Issues

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Swedish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿ Xi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1704-2017·2017-04-12

    Beckman Coulter Recalls AU680 and AU5800 Rack ID Labels Due to Mismatch

    Beckman Coulter is recalling Rack ID Labels for AU680 and AU5800 analyzers because the displayed ID number and barcode do not match.

    Product
    Beckman Coulter Chemistry Analyzer AU680/AU5800, Catalog No. MU907400 (Rack ID Labels) The Beckman Coulter AU680 and the AU5800 Clinical Chemistry Analyzers are an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibra
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0632-2017·2017-04-12

    Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination

    Alvogen, Inc. is recalling specific lots of Adalat CC (nifedipine) Extended-Release Tablets due to cross-contamination with sorafenib powder.

    Product
    Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 50419-70305
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1718-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Finnish SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1716-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Czech SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0628-2017·2017-04-12

    Adalat CC Tablets Recalled for Sorafenib Cross-Contamination

    Alvogen, Inc. is recalling Adalat CC (nifedipine) Extended Release Tablets 30 mg due to cross-contamination with sorafenib powder.

    Product
    Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1863-2017·2017-04-12

    McShare's Inc Recalls Premix Premix Due to Undeclared Soy

    McShare's Inc is recalling 700 lbs of Premack HS Vitamin RDA Premix because it contains low levels of undeclared soy.

    Product
    Premark HS Vitamin RDA Premix, Net Wt. 50 lbs., Item No. 136375.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1753-2017·2017-04-12

    Philips BrightView X Gamma Camera Recall Due to Brake Hub Assembly Error

    Philips Medical Systems is recalling 27 BrightView X gamma cameras because a brake hub assembly error can cause the detector to backdrive.

    Product
    BrightView X 3/8 model number 882478 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated, an
    Category
    Medical Device
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-1724-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Italian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1708-2017·2017-04-12

    Philips eCare Coordinator Software Recalled for Data Integrity Defects

    Philips Visicu is recalling eCare Coordinator software due to a defect that may cause missing or redundant data to be saved without user notification.

    Product
    eCare Coordinator Product Usage: is software intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through network
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1709-2017·2017-04-12

    Beckman Coulter Recalls Access 2 Immunoassay Systems Due to Circuit Board Defect

    Beckman Coulter is recalling Access 2 Immunoassay Systems because a defective circuit board can cause the device to stop running and cancel tests in process.

    Product
    Access 2 Immunoassay Systems, Part No. 81600N Product Usage: The Access 2 and UniCel DxI Access Immunoassay Systems are in vitro diagnostic devices used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1821-2017·2017-04-12

    Regeneca Recalls RegeneArouse Supplements for Manufacturing Violations

    VivaCeuticals is recalling all lots of RegeneArouse herbal and dietary supplements because they were not manufactured in compliance with current Good Manufacturing Practice regulations.

    Product
    RegeneArouse
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1714-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi English SRK.. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0634-2017·2017-04-12

    Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination

    Alvogen, Inc. is recalling Adalat CC (nifedipine) 60 mg extended-release tablets because residual sorafenib powder was found in the manufacturing facility's inlet air duct.

    Product
    Adalat CC (nifedipine) Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749501
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1749-2017·2017-04-12

    Siemens ADVIA Centaur BR Assay Recalled for Potential Syphilis Assay Interference

    Siemens is recalling ADVIA Centaur BR assays due to potential interference from the Syphilis assay, which may affect test accuracy.

    Product
    Siemens ADVIA Centaur BR assay Cat No. 09010686, SMN 10340081 (5-pack/250 tests - REF) BR Assay for CA 27.29 The ADVIA Centaur¿ BR assay is an in vitro diagnostic test for the quantitative serial determination of cancer antigen CA 27.29 in human serum using the ADVIA Centau
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1711-2017·2017-04-12

    Beckman Coulter Recalls UniCel DxC 600i SYNCHRON Access Clinical Systems

    Beckman Coulter is recalling specific UniCel DxC 600i SYNCHRON Access Clinical Systems because a circuit board defect can cause the device to stop running and cancel tests.

    Product
    UniCel DxC 600i SYNCHRON Access Clinical System, Part No. A25637, A25638 Product Usage: The Access 2 and UniCel DxI Access Immunoassay Systems are in vitro diagnostic devices used for the quantitative, semi-quantitative or qualitative determination of various analyte concentr
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1733-2017·2017-04-12

    Centurion Convenience Kits Recalled Due to Potential Sterile Packaging Breach

    Centurion Medical Products is recalling Convenience Kits containing Curity Oval Eye Pads due to a potential breach in sterile packaging.

    Product
    EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1715-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpreted instructions may cause tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Danish SRK. General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1747-2017·2017-04-12

    Siemens ADVIA Centaur BR Assay Recalled for Potential Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur BR assays due to potential interference from the Syphilis assay on the same systems.

    Product
    Siemens ADVIA Centaur BR assay Cat No. 02419937, SMN 10333349 (1-pack/50 tests) BR Assay for CA 27.29 The ADVIA Centaur¿ BR assay is an in vitro diagnostic test for the quantitative serial determination of cancer antigen CA 27.29 in human serum using the ADVIA Centaur¿, ADV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1725-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi EndoWrist Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi EndoWrist Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Korean SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vinci¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0649-2017·2017-04-12

    Dr. Reddy's Recalls Rivastigmine Tartrate Capsules Due to Cross-Contamination

    Dr. Reddy's is recalling Rivastigmine Tartrate Capsules because testing detected a peak for Ranitidine, indicating cross-contamination with other products.

    Product
    RIVASTIGMINE TARTRATE — RIVASTIGMINE TARTRATE (RIVASTIGMINE TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0633-2017·2017-04-12

    Alvogen Recalls Adalat CC Tablets Due to Sorafenib Cross-Contamination

    Alvogen is recalling specific lots of Adalat CC (nifedipine) extended-release tablets due to cross-contamination with sorafenib powder.

    Product
    Adalat CC (nifedipine) Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749401
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1720-2017·2017-04-12

    Intuitive Surgical Recalls da Vinci Xi Stapler Release Kits

    Intuitive Surgical is recalling da Vinci Xi Stapler Release Kits because misinterpretation of instructions may result in tool damage.

    Product
    STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit (SRK); model number 470298. da Vinci Xi Norwegian SRK General and Plastic Surgery: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45 Reloads and other Stapler Accessories are intended to be used with the da Vin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0636-2017·2017-04-12

    G & W Laboratories Recalls Ciclopirox Olamine Cream Due to Outdated Insert

    G & W Laboratories is recalling 230,700 tubes of Ciclopirox Olamine Cream because some lots were packaged with an out-of-date package insert.

    Product
    CICLOPIROX OLAMINE — CICLOPIROX OLAMINE (CICLOPIROX OLAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0630-2017·2017-04-12

    Alvogen Recalls Nifedipine Extended-Release Tablets Due to Cross-Contamination

    Alvogen, Inc. is recalling Nifedipine Extended-Release Tablets, 60 mg, due to cross-contamination with sorafenib powder found in the manufacturing facility's inlet air duct.

    Product
    Nifedipine Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-369-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V251000·2017-04-11

    Mercedes-Benz Recalls 2017 Models for Front Seat Belt Pretensioner Defect

    Mercedes-Benz is recalling 12,743 2017 vehicles because front seat belt pretensioners may not function properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S550, S550 4MATIC, C 300, GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V247000·2017-04-11

    Mercedes-Benz Recalls 2013 R320 Due to Post-Crash Fire Risk

    Mercedes-Benz is recalling one 2013 R320 4MATIC CDI vehicle because the engine may not shut off after a crash, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ R320
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V249000·2017-04-11

    Foretravel Recalls 2012-2018 Motorhomes Due to Front Suspension Defect

    Foretravel is recalling 2012-2018 Phenix, IH45, and Nimbus motorhomes because front suspension ball joints can loosen, potentially causing a loss of steering control.

    Product
    FORETRAVEL — FORETRAVEL NIMBUS, PHENIX, IH45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V241000·2017-04-11

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Water Ingress

    Mercedes-Benz is recalling specific 2016-2017 models because an insufficiently sealed electric power steering connector may allow water to enter the control unit, potentially deactivating steering assist.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GL350, GLE63S, GLE300D, GLE350D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V250000·2017-04-11

    Mercedes-Benz Recalls G-Class Vehicles for Steering Coupling Wear

    Mercedes-Benz is recalling 2013-2016 G550, G63, and G65 vehicles because an insufficiently tightened steering coupling may wear, potentially causing a loss of steering and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G63, AMG G65, G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V243000·2017-04-11

    Mercedes-Benz Recalls 2016-2017 C300 Vehicles for Steering Defect

    Mercedes-Benz is recalling 2016-2017 C300 vehicles because power steering motor contacts may be improperly welded, risking loss of steering assist and increased crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17739·2017-04-11

    John Deere Recalls Gator Utility Vehicles Due to Crash Hazard

    John Deere is recalling about 8,500 Gator Utility Vehicles because a loose dust boot on the throttle cable can prevent the vehicle from stopping, posing a crash hazard.

    Product
    Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V246000·2017-04-11

    Mercedes-Benz Recalls 2016-2017 E300 Vehicles for Spoiler Defect

    Mercedes-Benz is recalling 2016-2017 E300 and E300 4MATIC vehicles because the roof-mounted spoiler may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17129·2017-04-11

    Anaheim and Moen Recall Garbage Disposals Due to Impact Hazard

    Anaheim Manufacturing and Moen are recalling about 146,000 garbage disposals because a metal component can break off and exit the unit, posing an impact hazard.

    Product
    Garbage disposals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17128·2017-04-11

    Teavana Recalls Flip Tumblers Due to Hot Liquid Burn Hazard

    Starbucks is recalling Teavana Flip Tumblers because they can leak hot liquid, posing a burn risk. Consumers should stop using them and contact Starbucks for a refund.

    Product
    Teavana Flip Tumblers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V248000·2017-04-10

    Proline Cargo Trailer Recall for Short Wheel Nuts

    PROLine is recalling 2016-2017 Cargo trailers because short wheel nuts may allow wheels to detach, increasing crash risk.

    Product
    PROLINE — PROLINE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V239000·2017-04-10

    Thor Motor Coach Recalls 2017 Motorhomes Due to Incorrect Hitch Weight Labels

    Thor Motor Coach is recalling 2017 Ace, Hurricane, and Windsport motorhomes because tow hitch labels incorrectly state a 10,000 lb capacity instead of the actual 8,000 lbs.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR ACE, WINDSPORT, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V244000·2017-04-10

    Mercedes-Benz Recalls 2016 Metris for Front Seatbelt Pretensioner Defect

    Daimler Vans USA is recalling 2016 Mercedes-Benz Metris vehicles because front seatbelt pretensioners may not function properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V238000·2017-04-10

    Thor Motor Coach Recalls 2017 Palazzo Motorhomes for Incorrect Tire Labeling

    Thor Motor Coach is recalling 2017 Palazzo 36.1 and 36.3 motorhomes because the federal certification label lists an incorrect front tire rim size, which could lead to unsafe driving conditions if the rim is replaced based on that error.

    Product
    THOR — THOR PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·034-2017·2017-04-08

    Mibo Fresh Recalls Turkey Salad Due to Undeclared Allergens

    Mibo Fresh Foods is recalling approximately 3,434 pounds of ready-to-eat turkey salad products due to misbranding and undeclared allergens, including wheat and potential cross-contact with tree nuts, peanuts, soy, and milk.

    Product
    MIBO Fresh Foods LLC — Mibo Fresh Food Recalls Turkey Salad Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·17V236000·2017-04-07

    Altec Recalls 2004-2005 Aerial Devices Due to Boom Failure Risk

    Altec is recalling 2004-2005 aerial devices and elevators because the fiberglass upper boom may fail without warning, increasing the risk of serious injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V237000·2017-04-07

    Forest River Cherokee Recalled for Incorrect Federal Placard Weight Ratings

    Forest River is recalling 2007-2011 Cherokee recreational trailers because incorrect Federal Placards list higher weight ratings than the actual capacity, increasing the risk of overloading and crashes.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V233000·2017-04-06

    Mitsubishi Recalls 2016 Outlander Models for Door Latch Defect

    Mitsubishi is recalling 35,674 2016 Outlander and Outlander Sport vehicles because door latches may not secure in high temperatures, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17126·2017-04-06

    Marin Pine Mountain Bicycles Recalled Due to Fork Failure Hazards

    Marin Mountain Bikes is recalling 2016 and 2017 Pine Mountain bicycles because the front forks can bend or break, posing fall and crash hazards.

    Product
    Pine Mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V234000·2017-04-06

    Micro Bird Recalls 2016-2017 G5 School Buses for Fuel Valve Defect

    Micro Bird is recalling 2016-2017 G5 school buses with specific propane kits because a fuel valve may short circuit, causing the engine to shut off while driving.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1817-2017·2017-04-05

    Baidyanath Gaisantak Bati Recalled for Heavy Metal Contamination

    Butala Emporium, Inc. is recalling Baidyanath brand Gaisantak Bati dietary supplements because they contain lead, mercury, and/or arsenic at levels exceeding permissible limits.

    Product
    Baidyanath brand Gaisantak Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1720-2017·2017-04-05

    B & H Foods Recalls Ruth's Jalapeno Pimento Spread for Listeria Risk

    B & H Foods is recalling 3,394 units of Ruth's Jalapeno Pimento Spread due to potential Listeria monocytogenes contamination. The product was distributed in six southeastern states.

    Product
    Ruth's Jalapeno Pimento Spread, 12 oz. (UPC 74952-12014), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1727-2017·2017-04-05

    Seaquest Recalls Marinated Croaker Fish Due to Botulism Risk

    Seaquest Seafood Corp is recalling Sunrise Brand Marinated Silver/White Croaker because the product may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Marinated Silver/White Croaker - 30 x 14oz, Item No. C0081, UPC 5 08 54336-50081 0
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1417-2017·2017-04-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Failure to Deliver Therapy

    Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.

    Product
    HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1798-2017·2017-04-05

    Lipari Colby Jack Mini Horn Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Jack Mini Horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1724-2017·2017-04-05

    Sammy's Milk Baby Food Recalled for Cronobacter Bacteria

    Sammy's Milk is recalling specific lots of baby food due to possible Cronobacter bacteria and inadequate iron levels.

    Product
    Sammy's Milk (Baby Food), Net Wt. 12.84 oz (364 g), 6 containers per case
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1732-2017·2017-04-05

    Seaquest Recalls Dehydrated Big-Eye Herrings Due to Botulism Risk

    Seaquest Seafood Corp is recalling dehydrated Big-Eye Herrings because they may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Dehydrated Big-Eye Herrings - 1 x 3.3 lb, Item No. C0201, UPC 5 08 54336-50201 2
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1790-2017·2017-04-05

    Lipari Foods Recalls Colby Jack Cheese for Listeria Risk

    Lipari Foods is recalling Copper wood Colby Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Copper wood Colby Jack Mini Horn, 4/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1797-2017·2017-04-05

    Lipari Old Tyme Swiss Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Swiss Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Swiss Cheese, 2/8#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1777-2017·2017-04-05

    Saputo Recalls Dutchmark Smoked Gouda Cheese Due to Listeria Risk

    Saputo Cheese USA is recalling Dutchmark Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.

    Product
    Dutchmark, Pasteurized Processed Smoked Gouda Cheese. Product case Label: 989922 Dutchmark, Net Wt 24.00.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1688-2017·2017-04-05

    Gourmet Kitchen Recalls French Toast with Strawberries Due to Hepatitis A Risk

    Gourmet Kitchen, Inc. is recalling French Toast with Strawberries & Mascarpone because the frozen strawberries may be contaminated with Hepatitis A.

    Product
    Gourmet Kitchen Gourmet/Stuffed/French Toast with Strawberries & Mascarpone 20 PCS 1238 Corlies Avenue Neptune, NJ 07753 gourmetkitcheninc.com
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1729-2017·2017-04-05

    Seaquest Recalls Marinated River Barb Fish Due to Botulism Risk

    Seaquest Seafood Corp is recalling Sunrise Brand Marinated River Barb because it may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Marinated River Barb - 60 x 10 oz, Item No. C0140, UPC 2 08 54336-20140 2
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1741-2017·2017-04-05

    Ocho-Rios Jamaican Curry Powder Recalled for Lead Contamination

    Oriental Packing Co. is recalling Ocho-Rios Jamaican Nice Hot Curry Powder because the product contains lead.

    Product
    Ocho-Rios Jamaican Nice Hot Curry Powder, 4 oz. Manufactured by Oriental Packing Co.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1743-2017·2017-04-05

    Seafood Avenue Recalls Anchovy Products Due to Botulism Risk

    Seafood Avenue is recalling specific lots of anchovy products because they may support the growth of Clostridium botulinum, a pathogen that can produce toxins.

    Product
    DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162; B/C: 59033 50162
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1802-2017·2017-04-05

    Lipari Old Tyme Hot Pepper Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Hot Pepper Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Hot Pepper Cheese, 12/8 oz.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1794-2017·2017-04-05

    Lipari Old Tyme Colby Longhorn Cheese Recalled for Listeria Risk

    Lipari Foods is recalling specific lots of Old Tyme Colby Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Longhorn, 2/15#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1795-2017·2017-04-05

    Lipari Old Tyme Pepper Jack Mini Horn Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Pepper Jack Mini horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1792-2017·2017-04-05

    Lipari Old Tyme Colby Mini Horn Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Colby Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Mini Horn, 2/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1818-2017·2017-04-05

    Baidyanath Chitrakadi Bati Recalled for Heavy Metal Contamination

    Butala Emporium is recalling Baidyanath Chitrakadi Bati dietary supplements found to contain lead, mercury, and/or arsenic above permissible limits.

    Product
    Baidyanath brand Chitrakadi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1791-2017·2017-04-05

    Lipari Foods Recalls Copperwood Pepper Jack Mini Horn Cheese

    Lipari Foods is recalling Copperwood Pepper Jack Mini Horn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Copperwood Pepper Jack Mini Horn, 4/6#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1730-2017·2017-04-05

    Seaquest Recalls Dehydrated Anchovies Due to Botulism Risk

    Seaquest Seafood Corporation is recalling Sunrise Brand Dehydrated Anchovies because they may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Dehydrated Anchovy size 2/3cm - 1 x 22 lb, Item No. C0160, UPC 5 08 54336-50161 9
    Category
    Food
    Distribution
    0 states
  • CriticalUSDA FSIS·033-2017·2017-04-05

    Food Evolution Recalls Chicken Cous Cous Salad Due to Undeclared Pecans

    Food Evolution is recalling Mediterranean-style chicken cous cous salad because it contains undeclared pecans, a tree nut allergen.

    Product
    Food Evolution — Food Evolution, LLC. Recalls Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1731-2017·2017-04-05

    Seaquest Recalls Dehydrated Anchovies Due to Botulism Risk

    Seaquest Seafood Corp is recalling Sunrise Brand Dehydrated Anchovies because they may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Dehydrated Anchovy size 3/5cm - 100 x 3.5oz, Item No. C0161, UPC 2 08 54336-20161 9
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1725-2017·2017-04-05

    Life Rising DHZC-2 Chinese Herbal Supplement Recalled for Lead Contamination

    Life Rising Corp is recalling DHZC-2 Chinese Herbal Supplement tablets because the product contains lead. The recall covers 216 bottles distributed to nine US states.

    Product
    The product is packaged in a white plastic bottle with green lettering. The label reads in part "LIFE RISING DHZC-2, blood circulation regulator (lower abdomen), Chinese Herbal Supplement, 60 tablets, life rising to higher well being", UPC: 616042102727
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1742-2017·2017-04-05

    Ocho-Rios Mild Curry Powder Recalled for Lead Contamination

    Oriental Packing Co. is recalling Ocho-Rios Mild Curry Powder because the product contains lead. The recall affects 5 lb. packages sold in Jamaica and Florida.

    Product
    Ocho-Rios Mild Curry Powder, 5 lb. Manufactured by Oriental Packing Co.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1801-2017·2017-04-05

    Lipari Old Tyme Pepper Jack Cheese Recalled for Listeria Risk

    Lipari Foods is recalling Old Tyme Pepper Jack Cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Pepper Jack Cheese, 12/8 oz.
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1811-2017·2017-04-05

    Baidyanath Saptamrit Lauh Recalled for Heavy Metal Contamination

    Butala Emporium is recalling Baidyanath Saptamrit Lauh dietary supplements found to contain lead, mercury, and/or arsenic exceeding permissible limits.

    Product
    Baidyanath brand Saptamrit Lauh, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1810-2017·2017-04-05

    Baidyanath Rajahpravartini Bati Recalled for Heavy Metal Contamination

    Butala Emporium, Inc. is recalling Baidyanath brand Rajahpravartini Bati dietary supplements because they contain lead, mercury, and/or arsenic at levels exceeding permissible limits.

    Product
    Baidyanath brand Rajahpravartini Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1728-2017·2017-04-05

    Seaquest Recalls Marinated Climbing Perch Due to Botulism Risk

    Seaquest Seafood Corp is recalling Sunrise Brand Marinated Climbing Perch because the product may be contaminated with Clostridium botulinum.

    Product
    Sunrise Brand Marinated Climbing Perch - 30 x 16 oz, Item No. C0133, UPC 2 08 54336-20130 4
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1793-2017·2017-04-05

    Lipari Colby Jack Cheese Recalled for Listeria Contamination Risk

    Lipari Foods is recalling Old Tyme Colby Jack Longhorn cheese due to potential Listeria monocytogenes contamination from a supplier.

    Product
    Lipari Old Tyme Colby Jack Longhorn, 2/14.5#
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·F-1809-2017·2017-04-05

    Baidyanath Sarivadi Bati Recalled for Heavy Metal Contamination

    Butala Emporium, Inc. is recalling Baidyanath brand Sarivadi Bati dietary supplements because they contain lead, mercury, and/or arsenic at levels exceeding permissible limits.

    Product
    Baidyanath brand Sarivadi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
    Category
    Food
    Distribution
    10 states

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