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 661–680 of 47,938 recalls
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...
The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...
The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genepro Whey 4th Generation Plasma Treated Protein Recalled by Genepro...
The Issue: Product is mislabeled - the labeling contains incorrect ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Walgreens Saline Nasal Spray WITH XYLITOL Recalled by Medical Products...
The Issue: Microbial contamination of a non-sterile product - microorganism found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Stryker CranialMask Tracker is a single-use device consisting of...
The Issue: When the device is activated during surgery, the device software issues an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full...
The Issue: Affected gowns have the incorrect expiration date on the product packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. CAMHB W/LHB Recalled by Remel, Inc Due to Products may contain...
The Issue: Products may contain contamination, which may result in a darker or brown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath Recalled by Olympus Corporation of the Americas Due to...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and Recalled...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Resection Sheath Recalled by Olympus Corporation of the Americas Due...
The Issue: Complaints of the ceramic tip of the resection sheath breaking have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.