The Recall Desk

State

Rhode Island product recalls

73,827 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53776–53800 of 76881

  • 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (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
  • 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
  • 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 250E, B-CLASS ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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
  • 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
  • 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
  • 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-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-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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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 (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
  • 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 BAY STAR, BAY STAR SPORT, CANYON STAR
    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 DRY FREIGHT SEMI-TRAILER, CONVERTER DOLLY
    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·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
  • 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