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

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.

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 ...

A specific batch of extended-release Xanax failed a key quality test.

The U.S. Food and Drug Administration has listed a voluntary recall of a single lot of Xanax XR by a distributor of the medication, Viatris, Inc. Here's what this means.

Viatris initiated a voluntary recall of Xanax XR Lot 8177156 on March 17 after testing showed the tablets did not meet required dissolution specifications. The Food and Drug Administration has listed ...

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 ...

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.

Check your Xanax XR prescription: the FDA recalled one 3 mg batch after tablets failed standards for releasing the drug properly.