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. 2,526 recalls have been distributed to North Dakota in the last 12 months.
Showing 11461–11480 of 13,369 recalls
Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...
The Issue: Defective Delivery System; defective valve
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...
The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CUBICIN (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter: Customer complaint stating that one vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triveen - PRx RNF Capsules Recalled by Trigen Laboratories, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Label indicates that the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Product was out of specification (OOS) at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg Recalled by Pfizer...
The Issue: Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...
The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: Presence of Foreign Substance; some bottles may contain debris that was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...
The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Phenylephrine component is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength Recalled by...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Muro 128 (sodium chloride) hypertonicity ophthalmic ointment Recalled by...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....
The Issue: Failed Dissolution Specifications: Failure of dissolution test observed at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Hypertonicity Ophthalmic Ointment Recalled by Bausch & Lomb,...
The Issue: Crystallization: Crystal precipitate formation and an increase in the number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.