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.

Which agencies issued them

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.

53826–53850 of 76881

HighFDA (Devices)·Z-2824-2015·2015-10-07
Medtronic Navigated Solera Screwdrivers Recalled for Potential Tip Deformation
Medtronic Navigation is recalling 2,346 Navigated Solera Screwdrivers used in spine surgery because specific use conditions may cause the tips to deform or break.
Product
P/N: 9734856, SCREWDRIVER, 9734856, SOLERA STD MAST; P/N: 9734857, SCREWDRIVER, 9734857, SOLERA RDN MAST; P/N: 9734279, SCREWDRIVER 9734279 SOLERA STANDARD; and P/N: 9734373, SCREWDRIVER 9734373 SOLERA REDUCTION. The Medtronic Navigated Solera Screwdrivers are reusable devices…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0002-2016·2015-10-07
Biosense Webster Recalls Carto 3 EP Navigation System Due to Image Loss
Biosense Webster is recalling the Carto 3 EP Navigation System because the ultrasound image may disappear during use, requiring a system restart.
Product
Carto 3 EP Navigation System. Electro physiology system which views of the electrical activity of the heart through real-time data on 3-D, color-coded cardiac maps.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V630000·2015-10-07
Volvo Recalls 2015-2016 Trucks for Headlight Intensity Defect
Volvo is recalling 2015-2016 VAH and VHD trucks because some headlights do not meet federal intensity requirements, increasing crash risk.
Product
VOLVO — VOLVO VAH, VHD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-3257-2015·2015-10-07
KAL Amino Acid Complex Recalled for Undeclared Milk Allergen
Nutraceutical International is recalling KAL Amino Acid Complex because the ingredient list does not explicitly state 'milk,' despite containing casein.
Product
KAL Brand Amino Acid Complex UPC 021245 51610 1, Product #51610
Category
Food
Distribution
Distributed nationwide
HighCPSC·16701·2015-10-07
BRP Recalls Youth Can-Am ATVs Due to Fuel Filter Fire Hazard
BRP is recalling about 240 Youth Model Can-Am DS 90 and DS 90X ATVs because a fuel filter defect can cause leaks and fire. No injuries have been reported.
Product
Youth Model Can-Am all-terrain vehicles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2823-2015·2015-10-07
Medtronic Solera Screwdrivers Recalled for Tip Deformation Risk
Medtronic Navigation is recalling 2,346 Solera screwdrivers used in spine surgery because specific conditions may cause the tips to deform or break.
Product
P/N: 9735023, DRIVER 9735023 SOLERA 5.5/6.0 MAS; P/N: 9735024, DRIVER 9735024 SOLERA 5.5/6.0 MAS CAN; P/N: 9735025, DRIVER 9735025 SOLERA 5.5/6.0 RMAS; P/N: 9735026, DRIVER 9735026 SOLERA 5.5/6.0 RMAS CAN; P/N: 9735027,DRIVER 9735027 SOLERA 5.5/6.0 FAS/SAS. The Medtronic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2822-2015·2015-10-07
MicroAire LipoTower Recalled for Potential Electrical Shock Hazard
MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.
Product
ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2826-2015·2015-10-07
Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect
Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.
Product
Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2821-2015·2015-10-07
MicroAire LipoTower Recall Due to Electrical Shock Risk
MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.
Product
ASP-1020 LipoTower with Aspiration Pump. Medical use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2820-2015·2015-10-07
Zimmer Recalls Guide Wires Due to Incorrect Expiration Date Labeling
Zimmer, Inc. is recalling 112,568 sterile guide wires because the labels state a 10-year expiration date, while testing supports only 5 years.
Product
Zimmer Guide Wires for orthopedic procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0004-2016·2015-10-07
Lifeline Systems Recalls Philips GoSafe Mobile Help Button Due to Battery Issues
Lifeline Systems is recalling 8,616 Philips GoSafe Mobile Help Button devices because irregular battery disconnection can cause charging issues.
Product
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0005-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2819-2015·2015-10-07
Sterilmed Recalls Reprocessed Zimmer Tourniquet Cuffs Due to Mislabeling
Sterilmed is recalling 43 reprocessed Zimmer tourniquet cuffs because they are labeled as single hose but are actually dual hose devices.
Product
Zimmer, Reprocessed Zimmer Tourniquet Cuffs,34" Single Hose Single Bladder Brown (PLC), 34", Model (Reprocessor) Number: ZIM60-7075-106, Reprocessed by Sterilmed. Products are individually packaged in a Tyvek¿/poly pouch. There are 5 pouches placed inside a casepack box.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0001-2016·2015-10-07
Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2818-2015·2015-10-07
Olympus Recalls Gastrovideoscope Due to Insufficient Cleaning Accessory Information
Olympus is recalling 1,014 EVIS EXERA II Gastrovideoscopes because specific cleaning accessories required for reprocessing were not provided.
Product
EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0003-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, MEDIUM, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0004-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, TAN, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0002-2016·2015-10-07
Rodan & Fields Proactiv Foundation Recalled for Subpotent Salicylic Acid
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, LIGHT, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D1834-2015·2015-10-07
Apotex Recalls Verapamil Hydrochloride Extended-Release Tablets for Dissolution Failure
Apotex Inc. is recalling 2,075 bottles of Verapamil Hydrochloride Extended-Release tablets, 240 mg, because one lot failed to meet dissolution specification limits.
Product
Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V625000·2015-10-06
Winnebago and Itasca Motorhomes Recalled for Liquid Propane Hose Fire Risk
Winnebago is recalling 2013-2016 Era, Trend, Tour, Journey, and Itasca motorhomes because a liquid propane hose may harden and leak, increasing fire risk.
Product
WINNEBAGO — WINNEBAGO, ITASCA TREND, TOUR, JOURNEY, ERA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15E082000·2015-10-06
Dorman Aftermarket Steering Shafts Recalled for Potential Separation Risk
Dorman is recalling aftermarket steering shafts for 1995-2002 Ford, Mercury, and Lincoln vehicles because they may separate, causing loss of steering control.
Product
MERCURY — MERCURY, FORD, LINCOLN GRAND MARQUIS, CROWN VICTORIA, TOWN CAR
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16702·2015-10-06
Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Fire Hazard
Polaris is recalling approximately 53,000 RZR recreational off-highway vehicles because a misrouted fuel tank vent line can cause fuel leaks and fire.
Product
Recreational Off-Highway Vehicles (ROV)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V626000·2015-10-06
Kia Recalls 2011-2013 Sorento for Brake-Shift Interlock Defect
Kia is recalling 2011-2013 Sorento vehicles because the brake-shift interlock may fail, allowing the car to roll out of Park without the brake being pressed.
Product
KIA — KIA SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15E083000·2015-10-06
Meritor Recalls Axles Due to Loose Caliper Bolts
Meritor is recalling specific axle assemblies because caliper bolts may not be properly tightened. This defect could cause the caliper to detach, reducing braking performance and increasing crash risk.
Product
SERVICE BRAKES, AIR:DISC:CALIPER recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16700·2015-10-06
Sportsman's Guide Recalls Pop-Up Hunting Blinds Due to Fire Hazard
Sportsman's Guide is recalling about 17,000 pop-up hunting blinds because they are not made of flame-resistant materials, posing a fire hazard.
Product
Pop-up Hunting Blinds
Category
Consumer Product
Distribution
Distributed nationwide