The Recall Desk

State

Rhode Island product recalls

73,809 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.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42526–42550 of 76863

  • SevereFDA (Devices)·Z-0003-2018·2017-10-18

    St Jude Medical Recalls Fortify ICDs Due to Premature Battery Depletion

    St Jude Medical is recalling approximately 90,563 Fortify and Fortify Assura implantable cardioverter defibrillators because they may exhibit premature battery depletion.

    Product
    Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q; Fortify ST VR, Model Numbers: CD1241-40 and CD1241-40Q; Fortify Assura VR, Model Numbers: CD1257-40, CD1257-40Q, CD1357-40C, CD1357-40Q; Fortify Assura ST VR, Model Numbers: CD1263-40, CD1263-40Q, CD1363-40C, CD1363-40Q…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V661000·2017-10-18

    Navistar Recalls 2015-2018 IC Bus RE Due to Brake Hose Defect

    Navistar is recalling 2015-2018 IC Bus RE commercial buses because air brake hoses may contact tires, potentially causing brake failure or increased stopping distance.

    Product
    IC BUS — IC BUS RECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0004-2018·2017-10-18

    St Jude Medical Recalls Unify Cardiac Resynchronization Therapy Defibrillators

    St Jude Medical is recalling specific Unify and Quadra Assura cardiac resynchronization therapy defibrillators because they may exhibit premature battery depletion.

    Product
    Unify, Model Numbers: CD3231-40 and CD3231-40Q; Unify Quadra, Model Numbers: CD3249-40 and CD3249-40Q; Unify Assura, Model Numbers: CD3257-40, CD3257-40Q, CD3357-40C, CD3357-40Q; Quadra Assura, Model Numbers: CD3265-40, CD3265-40Q, CD3365-40C, CD3365-40Q; Quadra Assura MP, Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V657000·2017-10-18

    Toyota Recalls Sienna Minivans for Shift Lock Assembly Defect

    Toyota is recalling 2005-2007 and 2009-2010 Sienna vehicles because the shift lever may move out of Park without depressing the brake pedal, increasing crash risk.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V662000·2017-10-18

    Volkswagen Recalls 2018 Tiguans for Dim Back-up Lights

    Volkswagen is recalling 2018 Tiguans because the back-up lights may not be bright enough, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0021-2018·2017-10-18

    Birds Eye Baby Sweet Peas Recalled for Listeria Contamination Risk

    Pinnacle Food Group is recalling Birds Eye Baby Sweet Peas due to potential Listeria monocytogenes contamination. Consumers should check their freezers for the affected lots.

    Product
    Birds Eye Baby Sweet Peas, Net Wt. 13 oz. (369g ), Keep Frozen. UPC 14500-02253.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0011-2018·2017-10-18

    Abbott ARCHITECT c4000 Cuvette Segment Recall for Potential False Results

    Abbott is recalling 1,385 ARCHITECT c4000 cuvette segments because a detached post may cause falsely depressed patient results in adjacent cuvettes.

    Product
    ARCHITECT c4000 Cuvette Segment, List number 02P75-01. The firm name on the label is Abbott Laboratories, Abbott Park, IL. Cuvette segments are a component to the ARCHITECT c4000 system. Cuvette segments are racks that sit in the reaction carousel and hold cuvettes. Each…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0009-2018·2017-10-18

    Dr. Reddy's Recalls Famotidine Tablets Due to Impurity Failure

    Dr. Reddy's is recalling specific lots of famotidine tablets sold as CVS Pharmacy Acid Controller and Equate Famotidine due to an out-of-specification impurity result.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V655000·2017-10-17

    Mercedes-Benz Recalls 2016-2017 GLE and GLS Models for Air Bag Defect

    Mercedes-Benz is recalling 3,620 vehicles due to excess insulation that may interfere with the passenger air bag's protective function.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE63S, GLE350, GLE300D, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18010·2017-10-17

    Herman Miller Recalls Eames Fiberglass Rocking Chairs Due to Fall Hazard

    Herman Miller is recalling Eames fiberglass rocking chairs because the base can separate from the seat, posing a fall hazard. Nine fall reports were received, including six injuries.

    Product
    Eames fiberglass rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V651000·2017-10-16

    Mercedes-Benz Metris Recall for Front Wheel Bearing Defect

    Daimler Vans USA is recalling 2017 Mercedes-Benz Metris vans because front wheel bearings may not be seated correctly, risking wheel detachment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V654000·2017-10-16

    Mercedes-Benz Recalls AMG C63 Models for Rear Axle Defect

    Mercedes-Benz is recalling 2015-2017 AMG C63 vehicles because the rear axle differential mounting flange may fracture, potentially causing loss of propulsion and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V652000·2017-10-16

    Ford Recalls 2015-2017 F-Series Trucks for Door Latch Defect

    Ford is recalling 2015-2017 F-Series trucks because door latches may fail, allowing doors to open while driving and increasing injury risk.

    Product
    FORD — FORD F-550 SD, F-350 SD, F-250 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E060000·2017-10-16

    Nitrous Supply Recalls Prostar Solenoid Valves Due to Sleeve Breakage Risk

    Nitrous Supply is recalling Prostar Solenoid valves because end-stops on the sleeves may break under pressure, posing a risk of injury to nearby individuals.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V650000·2017-10-16

    Mercedes-Benz Recalls 2016 Sprinter Vehicles for Incorrect Load Capacity Label

    Daimler Vans USA is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vehicles because the B-pillar label may state a higher maximum load capacity than the vehicle is designed for.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V653000·2017-10-16

    Mercedes-Benz Recalls 2018 GLA 250 for Headlight Adjustment Issues

    Mercedes-Benz is recalling 2018 GLA 250 vehicles because low beam headlights may not meet federal safety standards, potentially reducing visibility.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·108-2017·2017-10-13

    Vermont Livestock Recalls Ground Beef Due To E. Coli O157:H7 Contamination

    Vermont Livestock Slaughter and Processing is recalling 133 pounds of ground beef sold at Bread & Butter Farm due to possible E. coli O157:H7 contamination linked to two illnesses.

    Product
    Vermont Livestock Slaughter And Processing LLC, Recalls Ground Beef Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide