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. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 26901–26920 of 48,376 recalls
Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lateral Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: radial stem implant #2 (Sterile packed). Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Extended Stem Size 2. Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp. Due...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lat Assembly Recalled by Howmedica Osteonics Corp. Due to Revision rate...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Standard Extended Stem Recalled by Howmedica Osteonics Corp. Due to...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radio Capitellum Small Recalled by Howmedica Osteonics Corp. Due to Revision...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee Spacer Blocks To assist in partial knee Recalled by...
The Issue: Zimmer Biomet is conducting a medical device recall for the Persona Partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is...
The Issue: Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GMK knee system: designed for cemented use in total Recalled by Medacta...
The Issue: Medacta has observed a worldwide occurrence rate of post-operative insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...
The Issue: Due to misinterpretation of the barcode by the scanner, when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...
The Issue: Possible open seal on top portion of the package. Could cause breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tortillas Recalled...
The Issue: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10...
Recommended Action: Do not consume. Return to store for a refund or discard.