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. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2076120780 of 27,884 recalls

Medical DeviceDecember 2, 2015· Skytron, Div. The KMW Group, Inc

Recalled Item: Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for...

The Issue: The hardware that holds the VESA plate and the display interface / monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 21 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· JosNoe Medical, Inc.

Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...

The Issue: Damage to package seals potentially compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Partners In Medicine Llc

Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...

The Issue: Device non-conformity which may lead to an incorrect oscillometric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Draeger Medical, Inc.

Recalled Item: Optional PS500 Power Supply Unit for the Evita V500 Ventilator Recalled by...

The Issue: The firm became aware of cases in which the battery run times of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· 3M Company - Health Care Business

Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...

The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...

The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Aesculap, Inc.

Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...

The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...

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

Class II — Potential Health HazardOngoing