Viatris, which Pfizer created in 2020, voluntarily withdrew extended-release products made at a plant in Ireland after an ...
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A specific batch of extended-release Xanax failed a key quality test.
The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...
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Xanax bottles recalled nationwide over dissolution issues
Bottles of Xanax are being recalled nationwide as they do not meet "dissolution specifications," according to the Food and ...
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.
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