The recall of the prescription-only anxiety medication was initiated by its distributor, Viatris, on March 17 ...

The anxiety medication is being recalled due to "failed dissolution specifications." ...

A specific lot of the widely prescribed anti-anxiety drug Xanax has been recalled nationwide for not passing quality control tests according to the Food and Drug Administration.

Viatris Specialty LLC initiated a nationwide retail-level recall of Xanax XR extended-release tablets, the company said in a notice to California’s Board of Pharmacy. The FDA classified the recall as ...

An allotment of Xanax distributed by a West Virginia-based company is being recalled nationwide, the U.S. Food and Drug Administration announced. Here’s what you need to know. A benzodiazepine, Xanax ...

If you take the prescription drug Xanax, you might want to consult your doctor before continuing to take it. A, Viatris, the manufacturer of Xanax, recalled 3-milligram extended-release tablets of ...

WASHINGTON, D.C. -- A nationwide recall has been issued for a specific lot of Xanax XR, a commonly prescribed anxiety medication, after federal regulators and the drug’s manufacturer flagged a ...

A batch of Xanax XR has been recalled nationwide after the manufacturer found the drug may not release properly in the body. The FDA classified the issue as moderate risk.

WASHINGTON, D.C. — A nationwide recall has been issued for a specific lot of Xanax XR, a commonly prescribed anxiety medication, after federal regulators and the drug’s manufacturer flagged a ...

Pharmaceutical company Viatris Specialty LLC voluntarily recalled one lot of Xanax XR (alprazolam extended-release 3 mg) tablets on March 17, 2025, after routine quality testing revealed the pills ...