Viatris Inc recalls
9 recalls on record · FDA
Every recall we have on record for Viatris Inc, compiled from federal safety data. Check the hazard, the remedy, and how serious each one is, and always confirm on the official notice.
Levothyroxine Sodium Tablets USP, 150 mcg, packaged in a) 90-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
Levothyroxine Sodium Tablets USP, 50 mcg, packaged in a) 90-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
Levothyroxine Sodium Tablets USP, 125 mcg, packaged in a) 90-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
Levothyroxine Sodium Tablets USP, 200 mcg, packaged in a) 90-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
Levsin injection (hyoscyamine sulfate injection, USP), 0.5 mg per ml in water for…
CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials…
Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only,…
Failed Dissolution Specifications: low out of specification results for dissolution.
alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by:…
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.