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. 1,043 recalls have been distributed to North Dakota in the last 12 months.
Showing 11041–11060 of 47,938 recalls
Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Whitening Mouthwash Recalled by Family Dollar Stores, Llc. Due to...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...
The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...
The Issue: Identification of an unknown impurity at the 12-month stability point....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...
The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...
The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...
The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.