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. 902 recalls have been distributed to North Dakota in the last 12 months.
Showing 44621–44640 of 47,938 recalls
Recalled Item: Edetate Disodium Injection Recalled by FVS Holdings, Inc. dba. Green Valley...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexpanthenol Injection Recalled by FVS Holdings, Inc. dba. Green Valley...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Edetate Calcium Disodium Injection Recalled by FVS Holdings, Inc. dba. Green...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pyridoxine Hydrochloride Injection Recalled by FVS Holdings, Inc. dba. Green...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Injection Recalled by FVS Holdings, Inc. dba....
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Injection Recalled by FVS Holdings, Inc. dba. Green Valley...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxocobalamin Injection Recalled by FVS Holdings, Inc. dba. Green Valley...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polidocanol Injection Recalled by FVS Holdings, Inc. dba. Green Valley Drugs...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Injection Recalled by FVS Holdings, Inc. dba. Green Valley...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Injection Recalled by FVS Holdings, Inc. dba. Green...
The Issue: Lack of Assurance of Sterility: all sterile products compounded, repackaged,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3536A Recalled by...
The Issue: Device Operating on Battery Power May Shutdown without Warning if exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an...
The Issue: Several complaints were recorded regarding one of the three screws driving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: Cartridges may contain individual discs which were not impregnated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103...
The Issue: Alpine Biomed ApS is recalling Natus neurology Dantec KEYPOINT.NET ver. 2.20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL RecombiPlasTin 2G Recalled by Instrumentation Laboratory Co. Due to...
The Issue: Instrumentation Laboratory is recalling HemosIL RecombiPlasTin 2G (RPT2G),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-First Brand First Aid Kit Recalled by Total Resources Intl Due to CGMP...
The Issue: CGMP Deviations: The first aid kits that are subject to the voluntary recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.