FDA Drugs recall ·
Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles… recall
- Recall number
- D-0444-2026
- Date
- (initiated March 17, 2026)
- Company / brand
- Viatris Inc
1000 Mylan Blvd, Canonsburg, PA, United States - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Failed Dissolution Specifications
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot# 8177156, Exp Date: 02/28/2027
Distribution
US Nationwide.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0444-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.