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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,560 in last 12 months

Showing 34613480 of 47,970 recalls

FoodDecember 9, 2024· Riverside Natural Foods, Ltd.

Recalled Item: 1. Cookies & Creme Granola Bars 30.6oz (36 bars) 2. Recalled by Riverside...

The Issue: may contain metal pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2024· Riverside Natural Foods, Ltd.

Recalled Item: 1. MadeGood Chocolate Chip Granola Bars 34oz (40 bars) 2. Recalled by...

The Issue: may contain metal pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2024· Riverside Natural Foods, Ltd.

Recalled Item: Chocolate Chip Granola Mini Bars Recalled by Riverside Natural Foods, Ltd....

The Issue: may contain metal pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2024· Riverside Natural Foods, Ltd.

Recalled Item: 1. Chocolate Drizzled Cookie Crumble Granola Bars 4.2oz (5 bars) Recalled by...

The Issue: may contain metal pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 9, 2024· Borsari Food Company Inc

Recalled Item: BORSARI Food Company Incorporated Recalled by Borsari Food Company Inc Due...

The Issue: Product contains undeclared fish (anchovy) and soy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 9, 2024· Maquet Cardiovascular, LLC

Recalled Item: VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers:...

The Issue: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2024· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model...

The Issue: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone...

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

Class I — Serious Health HazardOngoing
DrugDecember 6, 2024· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Amerisource Health Services LLC

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Amerisource Health Services...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Amerisource Health Services LLC

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Amerisource Health...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Amerisource Health Services LLC

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Amerisource Health...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Amerisource Health Services LLC

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Amerisource Health Services...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2024· Aurobindo Pharma USA Inc

Recalled Item: Nebivolol Tablets Recalled by Aurobindo Pharma USA Inc Due to CGMP...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2024· DDS Lab

Recalled Item: Temporary Titanium Abutments Recalled by DDS Lab Due to Certain definitive...

The Issue: Certain definitive dental implant restoration cases may have included a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2024· GE Medical Systems, LLC

Recalled Item: Portrait Core Services Recalled by GE Medical Systems, LLC Due to There is a...

The Issue: There is a software issue that can result in the loss of patient monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2024· QUIDEL ORTHO

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Hemoglobin interference may occur at concentrations lower than the claimed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2024· QUIDEL ORTHO

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Hemoglobin interference may occur at concentrations lower than the claimed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Dialyzer Optiflux 160NRe Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: Potential for internal blood leaks due to cracked polyurethane

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Reconstruction System Neck Segment (with suture holes Recalled by...

The Issue: Error on the main label and the patient label. The labels indicate a size...

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

Class II — Potential Health HazardOngoing