FDAFDA · Food and drugs·Recall number D-0444-2026
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
Published April 15, 2026 · Recall initiated: March 17, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Dissolution Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- XANAX
- Manufacturer
- Viatris, Inc.
- Distributor
- US Nationwide.
- UPC
- 0358151506910
- Lot
- Lot# 8177156, Exp Date: 02/28/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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