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FDA · Drugs ·

Xanax XR, alprazolam recall

Viatris, Inc. recalled Xanax XR, alprazolam on April 15, 2026 because of failed dissolution specifications. It was sold nationwide.

Why it was recalled

Failed Dissolution Specifications

What's recalled

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

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Viatris, Inc., Canonsburg, PA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0444-2026
Source
U.S. Food and Drug Administration

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