Class II · ModerateActive recall
Xanax
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot# 8177156, Exp Date: 02/28/2027
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Failed Dissolution Specifications
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byMade in Ireland foreign manufacturer
| Brand name | XANAX |
| Generic name | ALPRAZOLAM |
| Active ingredient(s) | ALPRAZOLAM |
| Distributed by / for | Viatris Specialty LLC, Morgantown, WV 06506, U.S.A |
| NDC | 58151-506-91 |
Show the full FDA record
| Full product label | 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 |
| Recalling firm | Viatris, Inc. |
| Distribution | US Nationwide. |
| Recall initiated | 2026-03-17 |
| Report date | 2026-04-15 |
| Recall completed | — |
| Recall number | D-0444-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Canonsburg PA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.