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. 2,473 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,473 in last 12 months

Showing 1480114820 of 27,884 recalls

Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...

The Issue: There is a possibility that the liquid suction pump on some AIA-2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph mCT: a) S(64)-3R Recalled by Siemens Medical Solutions USA, Inc....

The Issue: The terminals on the plug may become loose and overheat.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...

The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing