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. 2,510 recalls have been distributed to North Dakota in the last 12 months.
Showing 12781–12800 of 13,369 recalls
Recalled Item: 4 way Nasal Decongestant Fast Acting Nasal Spray Recalled by Novartis...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Menthol Nasal Spray Recalled by Novartis Consumer...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Saline Moisturizing Mist with Eucalyptol & Menthol Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifadin Recalled by Sanofi US Due to Subpotent drug: low fill volume in some...
The Issue: Subpotent drug: low fill volume in some of the capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myoflex (trolamine salicylate) 10% Recalled by Novartis Consumer Health Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nupercainal Recalled by Novartis Consumer Health Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.