Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,042 recalls have been distributed to Rhode Island in the last 12 months.
Showing 14121–14140 of 47,970 recalls
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA Versions: 4.7 Recalled by BioMerieux SA Due to Under certain...
The Issue: Under certain conditions, there is a risk for a false negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health Daytime Severe Cold & Flu Relief Single-Use Vials Recalled by New...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 Recalled by New...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. Recalled by...
The Issue: Product mispackaging; mixed nuts (cashews, macadamia, and walnuts) packed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRULIANT Knee System including TRULIANT Tibial Inserts Recalled by Exactech,...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...
The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.