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." ...

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 ...

U.S. Food and Drug Administration issues a recall notice of an allotment of Xanax over dissolution failure.

A widely used anxiety medication is being pulled from shelves due to "failed dissolution specifications," the U.S. Food and Drug Administration (FDA) said. The agency's enforcement report said that ...

(Gray News) - Xanax, a popular prescription anxiety medication, has been recalled nationwide, according to the Food and Drug Administration. On March 17, the distributor recalled 3-milligram tablets ...

A single batch of the widely prescribed antianxiety drug Xanax has been recalled, according to the Food and Drug Administration. The drug’s distributor, Viatris, said it was recalling one lot ...

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 ...

News of an anxiety medication recall has raised concern among patients, caregivers, and healthcare providers across the United States. For many people, medications used to manage anxiety are part of ...

The recall, issued March 17, affects lot number 8177156. The bottles contain 60 tablets of the 3-milligram extended-release version of the prescription drug, with an expiration da ...