Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,577 recalls have been distributed to Delaware in the last 12 months.
Showing 16241–16260 of 27,373 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: 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: 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: 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: 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: 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: 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 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: #2 Bipolar stem implant (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 Stem Implant 6mm Collar 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: radial head 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: 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: 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: 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: 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.