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. 2,563 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,563 in last 12 months

Showing 921940 of 48,376 recalls

Medical DeviceOctober 24, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There were instances where the operator table was sold together with a...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Bromocriptine Mesylate Capsules Recalled by Zydus Pharmaceuticals (USA) Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2025· Datascope Corp.

Recalled Item: Cardiosave Rescue Recalled by Datascope Corp. Due to The IFU addendum...

The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2025· Datascope Corp.

Recalled Item: Cardiosave Hybrid Recalled by Datascope Corp. Due to The IFU addendum...

The Issue: The IFU addendum updates the Vibration and Shock Table to the correct standards.

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2025· Becton Dickinson & Co.

Recalled Item: BD Kiestra" Isolate Suspension Cuvette Array Recalled by Becton Dickinson &...

The Issue: The 2D barcodes on these cuvettes contain formatting errors that prevent the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

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

Class II — Potential Health HazardOngoing
Refund