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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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