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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,521 in last 12 months

Showing 94019420 of 47,970 recalls

DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Aripiprazole 5mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Rosuvastatin 10mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2023· RemedyRepack Inc.

Recalled Item: Ropinirole 0.5 mg tablets Recalled by RemedyRepack Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 20, 2023· Wismettac Asian Foods, Inc.

Recalled Item: FURIKAKE SEASONED ROASTED SEAWEED FLAKES SPICY Product #38246 Brand name:...

The Issue: Product was found to have the incorrect crustacean named on products

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 20, 2023· Wismettac Asian Foods, Inc.

Recalled Item: FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand...

The Issue: Product was found to have the incorrect crustacean named on products

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 20, 2023· Philips North America

Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813...

The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2023· Philips North America

Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814...

The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2023· DermLite LLC

Recalled Item: DERMLITE DL4W Recalled by DermLite LLC Due to Incorrect labeling; Package...

The Issue: Incorrect labeling; Package labeling contains a different serial number then...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Ascend Laboratories, LLC

Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Out of...

The Issue: Out of specification (OOS) for Spectroscopic Identification test by IR.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 17, 2023· Perrigo Nutritionals

Recalled Item: Gerber GoodStart SoothePro Infant Formula with Iron. Milk Based Powder....

The Issue: Infant Formula has the potential to be contaminated with Cronobacter spp.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 17, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...

The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Beaver Visitec International, Inc.

Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....

The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Medtronic Neuromodulation

Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...

The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Tadalafil Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: BusPIRone Hydrochloride Tablets USP Recalled by Northwind Pharmaceuticals...

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund