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. 2,461 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,461 in last 12 months

Showing 1412114140 of 47,970 recalls

DrugSeptember 2, 2021· New Vision Pharmaceuticals LLC

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.

Class III — Low RiskOngoing
Refund
DrugSeptember 2, 2021· New Vision Pharmaceuticals LLC

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.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· BioMerieux SA

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.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 2, 2021· Abbott Molecular, Inc.

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.

Class I — Serious Health HazardOngoing
FoodSeptember 1, 2021· Andersen & Sons Shelling, Inc.

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2021· Medtronic Xomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

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.

Class II — Potential Health HazardOngoing