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 34013420 of 47,970 recalls

DrugDecember 16, 2024· SHOPPERS- PLAZA

Recalled Item: FOUZEE SugarLin HERBAL FORMULA capsules Recalled by SHOPPERS- PLAZA Due to...

The Issue: Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 16, 2024· FDC Limited

Recalled Item: Ciprofloxacin Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: Unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2024· SOMERSET THERAPEUTICS LLC

Recalled Item: Atropine Sulfate Ophthalmic Solution Recalled by SOMERSET THERAPEUTICS LLC...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· Olympus Corporation of the Americas

Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...

The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2024· Alphatec Spine, Inc.

Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...

The Issue: Complaints have been received regarding post-operative implant collapse.

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

Class II — Potential Health HazardOngoing
DrugDecember 13, 2024· Amerisource Health Services LLC

Recalled Item: Clobazam Tablets Recalled by Amerisource Health Services LLC Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...

The Issue: Potential for hole in package compromising sterility of the medical kit.

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2024· Akron Pharma, Inc.

Recalled Item: Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere...

The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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

Class III — Low RiskOngoing
Refund