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. 2,336 recalls have been distributed to West Virginia in the last 12 months.
Showing 34161–34180 of 48,376 recalls
Recalled Item: ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro Recalled by Horiba...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender PFJ FEMORAL COMP Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Lactic Acid CP ref. A11A01721 reagent is intended Recalled by...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul Head 40 Recalled by Zimmer Biomet, Inc. Due to LDPE bag containing...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Uric Acid CP ref. A11A01670 is an in Recalled by Horiba...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 7.5 INCH BEADED FC prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-FLEX Option FEM NexGen CR-FLEX Precoat FEM NexGen CR-FLEX Recalled...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...
The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRCT MIS CR MOB PLT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specify 5-6-5 Lead Recalled by Medtronic Neuromodulation Due to Some Specify...
The Issue: Some Specify 5-6-5 and 2x8 surgical lead product labeling does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NKII CSTI Porous Femoral NKII NP Femoral prosthesis Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 VERSYS 6 INCH BEADED Recalled by Zimmer Biomet,...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Knee LPS Porous FEM NexGen Knee LPS Option FEM Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABX PENTRA Cholesterol CP ref. A11A01634 is an in Recalled by Horiba...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tiger King Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weekend Prince Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.