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. 1,037 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,037 in last 12 months

Showing 16381–16400 of 47,970 recalls

Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 10.0MM REAMER HEAD FOR RIA 2 Recalled by Synthes (USA)...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 13.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 15.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 17.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 17.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...

The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Philips North America, LLC

Recalled Item: Emission Computed Tomography System Image Process System - Product Usage:...

The Issue: A software defect that has the potential to result in image misdiagnosis and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Roche Molecular Systems, Inc.

Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...

The Issue: Dirty Lens May Cause Invalid or False Positive Results

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Lidco Ltd

Recalled Item: CM 50-001-01 Injectate Kit Recalled by Lidco Ltd Due to The expiration date...

The Issue: The expiration date on labeling is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2020· Steris Corporation

Recalled Item: Medisafe Distal Duck Kit and Duck Bag Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that certain lots of diluted 4-Zyme may contain...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2020· Areva Pharmaceuticals Inc

Recalled Item: Irinotecan Hydrochloride Injection Recalled by Areva Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: based on a Warning Letter received by the manufacturer of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2020· US Pharmaceuticals Inc.

Recalled Item: CVS Health Hydrating Healing Ointment (Petrolatum 41%) Recalled by US...

The Issue: Lack Of CGMP:s Low weight fill tubes were identified in one lot of CVS...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2020· Fusion Health and Vitality LLC

Recalled Item: Immune Boost with natural strawberry flavor Recalled by Fusion Health and...

The Issue: Marketed without an Approved NDA/ANDA: Product marketed with drug claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2020· The Harvard Drug Group

Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceRod" 1.5 PLUS 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Becton Dickinson & Company

Recalled Item: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) Recalled by Becton...

The Issue: BD has confirmed the presence of blood on the cannulas of the BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSphere" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSphere" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSphere" 1.5 S 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: Three IceFORCE" 2.1 CX Prostate Cryoablation Kit Recalled by Boston...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceRod" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing