Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,943 recalls have been distributed to Virginia in the last 12 months.
Showing 17421–17440 of 29,425 recalls
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...
The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fastener Recalled by Zimmer Biomet, Inc. Due to It was identified that the...
The Issue: It was identified that the product was not assembled correctly causing the...
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: 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: rHead Recon Extended Stem Size 1. 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 non-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: #2 Bipolar radial head Implant (Sterile packed). Orthopedic implant for...
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 Large 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: Radio Capitellum 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 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: 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 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.