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.

Bottles of Xanax have been recalled after failing a quality control test, according to the Food and Drug Administration. Bottles of Xanax – one of the most widely-prescribed medications for anxiety – ...

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.

The U.S. Food and Drug Administration has updated the risk level for a popular anxiety medication that was recalled nationwide. The agency recently classified Xanax XR, alprazolam, extended-release ...

The FDA has designated it a class II recall.

· The FDA announced a voluntary recall of select lots of Xanax. · The impacted lots may dissolve too quickly or not fast enough in the body. · Patients who have concerns should contact their doctor.

Bottles of a popular medication used to treat anxiety and panic disorders are being recalled nationwide, according to a report from the Food and Drug Administration. One lot of Xanax, one of the most ...

The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, which could make the drug less effective. Experts advise continuing your ...

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

Bottles of Xanax – one of the most widely-prescribed medications for anxiety – have been recalled after failing a quality-control test, according to the Food and Drug Administration. Viatris, Inc., a ...