The FDA has designated it a class II recall.
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.
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 is recalled due to improper dissolution, posing potential health risks. The FDA advises patients to consult their doctors for alternatives.
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Anxiety medication Xanax recalled nationwide, according to FDAThe anxiety medication is being recalled due to "failed dissolution specifications." ...
NEW YORK (WPIX) – A widely prescribed medication for treating anxiety and panic disorders is being recalled nationwide, according to the U.S. Food and Drug Administration. A specific lot of ...
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 ...
U.S. Food and Drug Administration issues a recall notice of an allotment of Xanax over dissolution failure.
If you take the prescription drug Xanax, you might want to consult your doctor before continuing to take it. According to the U.S. Food and Drug Administration, Viatris, the manufacturer of Xanax, ...
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.
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 ...
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 ...
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