Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,537 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,537 in last 12 months

Showing 54215440 of 27,884 recalls

Medical DeviceOctober 4, 2023· Baxter Healthcare Corporation

Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...

The Issue: Progressa+ beds have the potential for static buildup from the casters...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2023· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...

The Issue: Elevated results were detected with Li-heparin plasma samples when compared...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: DRX Revolution Mobile X-Ray System Recalled by Carestream Health, Inc. Due...

The Issue: Unexpected failure of electrical components within the CPI generator.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Carestream Health, Inc.

Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...

The Issue: There is a potential for unexpected failure of the electrical components...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...

The Issue: Sterilization failures when devices are sterilized per the Reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Olympus Corporation of the Americas

Recalled Item: ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI Recalled by...

The Issue: Incorrect pouch labels, the contents within the mislabeled pouch were Roller...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Coapt LLC

Recalled Item: Coapt Dome Electrode Recalled by Coapt LLC Due to Patient may experience...

The Issue: Patient may experience minor burn or blistering if device is exposed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Stanbio Laboratory, LP

Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...

The Issue: Deterioration in the stability of the Test Strips results in diminished...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2023· Edge Biologicals Inc

Recalled Item: Edge Biologicals STERILE WATER Recalled by Edge Biologicals Inc Due to Due...

The Issue: Due to product outer packaging incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: Alinity c Iron Reagent Recalled by Sentinel CH SpA Due to A high recovery of...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Sentinel CH SpA

Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...

The Issue: A high recovery of Iron assay has been observed at some customer sites....

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

Class II — Potential Health HazardOngoing