Class II
Ongoing
Levothyroxine Sodium Tablets USP, 200 mcg, packaged in a) 90-count bottles (NDC 0378-1819-77) and b) 1000-count bottles (NDC 0378-1819-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.
This recall is currently active, issued December 18, 2024. It was issued by Viatris Inc.
- Company
- Viatris Inc
- Recall Initiated
- November 18, 2024
- Posted
- December 18, 2024
- Recall Number
- D-0122-2025
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 55,032 bottles
- Firm Location
- Canonsburg, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Superpotent Drug and Subpotent Drug: potency failures obtained
Distribution
Nationwide within the United States and Puerto Rico
Lot / Code Info
Lot #: a)8179847, Exp. Date July 2025; b) 3203518, Exp. Date July 2025
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