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. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 601–620 of 47,938 recalls
Recalled Item: Cisatracurium Besylate Injection USP Recalled by SOMERSET THERAPEUTICS LLC...
The Issue: Subpotent product:out of specification assay results observed during long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL) Recalled by...
The Issue: Correct Labeled Product Mispack-Size stated on carton label did not match...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...
The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...
The Issue: Butyrate tube cracks during actuation, rendering product unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: For certain customers, the Change Summary review option ceases to operate as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Vapor 2000. Unheated Recalled by Draeger, Inc. Due to A certain...
The Issue: A certain component of affected devices was not delivered within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: Software issue only allows Concentration Limits to be defined to one digit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to...
The Issue: Ophthalmic procedure packs may have incomplete seals affecting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Vapor 3000. Unheated Recalled by Draeger, Inc. Due to A certain...
The Issue: A certain component of affected devices was not delivered within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.