Viatris, Inc. recalls Xanax XR
- Recalling company
- Viatris, Inc.
- Product
- Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91
- Reason
- Failed Dissolution Specifications
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 17, 2026
- Reported
- Apr 15, 2026
- Distribution
- US Nationwide.
- Status
- Ongoing
- Lot / codes
- Lot# 8177156, Exp Date: 02/28/2027
- Company location
- Canonsburg, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0444-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0444-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.