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.
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.
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 ...
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 ...
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, ...
· The impacted lots may dissolve too quickly or not fast enough in the body. · Patients who have concerns should contact their doctor. The Food and Drug Administration has announced a voluntary recall ...
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 ...
A specific allotment of the medication Xanax, typically prescribed to treat mental health challenges including anxiety and panic disorders, has been recalled due to the product’s potential to cause ...
One Lot of Xanax Recalled Nationwide Over Quality Issue, FDA Says By HealthDay Staff HealthDay ReporterTHURSDAY, April 16, 2026 (HealthDay News) — A widely used anxiety medication is being pulled from ...