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. 2,539 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,539 in last 12 months

Showing 52815300 of 47,970 recalls

FoodMay 31, 2024· Natural Organics, Inc.

Recalled Item: NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost for Men 60...

The Issue: Product is missing the ingredient TongKat Ali and has additional Rhodiola Rosea

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

Class III — Low RiskOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size) Recalled by...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Blue Ventilator Adapter Module. Intermittent positive...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential for certain Life2000 ventilator systems to either fail to charge...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Integra LifeSciences Corp.

Recalled Item: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical...

The Issue: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
FoodMay 28, 2024· U.B.C. Food Distributors INC.

Recalled Item: Baraka brand ground black pepper packaged in 7oz retail containers Recalled...

The Issue: Potential Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 28, 2024· Consumer Product Partners, LLC

Recalled Item: Petroleum Jelly Recalled by Consumer Product Partners, LLC Due to Labeling:...

The Issue: Labeling: Label Mix up; product labeled as pure white petroleum jelly...

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

Class II — Potential Health HazardOngoing
Refund