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Story summary
- The U.S. Food and Drug Administration announced a voluntary recall of a single Viatris-distributed Xanax XR 3 mg extended-release tablet lot after dissolution issues could reduce efficacy.
- Viatris initiated the recall on March 17, 2026, after internal testing identified the dissolution defect.
- This is not Xanax XR’s first recall, with related problems in 2012 and 2022.
- No injuries have been reported, but the recall raises concerns about trust in anxiety medicines.
