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. 1,071 recalls have been distributed to Delaware in the last 12 months.
Showing 5081–5100 of 48,330 recalls
Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...
The Issue: Affected product has an increased risk of postoperative perisprosthetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Cross contamination with other products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...
The Issue: Cross contamination with other products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...
The Issue: Cross contamination with other products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Cross contamination with other products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PEG-3350 Recalled by Novel Laboratories, Inc. d.b.a Lupin Somerset Due to...
The Issue: Defective container: potential for non-sealed pouches which can lead to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Failed Dissolution Specifications: results below specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fludrocortisone Acetate Tablets Recalled by Teva Pharmaceuticals USA, Inc...
The Issue: Failed Impurities/Degradation Specifications: Product is being recalled due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.