Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Xanax XR (alprazolam) extended-release tablets Recalled by Viatris Inc Due to Failed Dissolution Specifications: low out of specification results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.
Affected Products
Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer Inc, NY, NY 10017, NDC 0009-0068-07.
Quantity: 110 bottles
Why Was This Recalled?
Failed Dissolution Specifications: low out of specification results for dissolution.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris Inc
Viatris Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report