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. 2,469 recalls have been distributed to Delaware in the last 12 months.
Showing 24401–24420 of 27,373 recalls
Recalled Item: GE Healthcare - Giraffe and Panda Bag and Mask Resuscitation System Recalled...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System Recalled by...
The Issue: Toshiba intitiated this recall because their investigation revealed that due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare - Giraffe Warmer Recalled by GE Healthcare, LLC Due to Oxygen...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker...
The Issue: Stryker received a report from the field indicating that a 5.5 mm Cancellous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare - Giraffe¿ and Panda¿ iRes Infant Warmer Product Recalled by...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blom-Singer Adjustable Tracheostoma Valve II Models: BE8025H and BE8025H-R3...
The Issue: InHealth Technologies (IHT) is recalling the Blom-Singer Adjustable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Recalled...
The Issue: Stryker has received complaints associated with cracks and/or fracture of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified customers regarding over stimulation or stimulation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine...
The Issue: Custom Procedural Trays/Kits contain 1% Lidocaine HCl injection which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard LifeStent Solo Vascular Stent Recalled by Bard Peripheral Vascular Inc...
The Issue: Bard Peripheral Vascular is recalling specific lots of Bard Lifestent Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...
The Issue: During aging studies, the firm determined that the gastric belts were unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM Recalled...
The Issue: Stryker has received complaints associated with cracks and/or fracture of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified customers regarding over stimulation or stimulation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Recalled by...
The Issue: A potential non conformance was identified with the Zero-P VA plate where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...
The Issue: During aging studies, the firm determined that the gastric belts were unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by...
The Issue: Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...
The Issue: During aging studies, the firm determined that the gastric belts were unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod Insulin Management System Starter Kit Recalled by Insulet...
The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.