Viatris has recalled one lot of Xanax nationwide after the anxiety medication failed dissolution specifications, the FDA announced March 17. The recall affects lot number 8177156, which contains 60 tablets of the 3-milligram extended-release version with an expiration date of February 28, 2027. The tablets may not properly break down and release the drug into the body as intended, potentially causing reduced effectiveness or inconsistent dosing. The FDA classified this as a Class II recall, meaning use may cause temporary or medically reversible health consequences, with remote probability of serious adverse effects.
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