Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,762 recalls have been distributed to North Dakota in the last 12 months.
Showing 31961–31980 of 47,938 recalls
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...
The Issue: Sterility compromised due to breach in sterile packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection Recalled by Talon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...
The Issue: Failed Dissolution Specifications: out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Injection (a) 2500 iu Recalled by Talon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...
The Issue: Failed Dissolution Specifications: out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bactroban Nasal Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bactroban Ointment Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Original Bacon Flavored Seasoning Salt Recalled by J&D's Down Home...
The Issue: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Theo Chocolate Salted Almond 70% Dark Chocolate bars are wrapped Recalled by...
The Issue: The Salted Almond 70% Dark Chocolate bars are recalled due to undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MACH AxiEM Cranial Treon. The software application is sent in Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...
The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.