The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, ...

The FDA has confirmed a nationwide Class II recall of a specific lot of Xanax XR (alprazolam extended-release) after it failed dissolution tests, raising concerns about dosage consistency and ...

Viatris, which Pfizer created in 2020, voluntarily withdrew extended-release products made at a plant in Ireland after an ...

If you have a bottle of Xanax XR at home, it is worth checking the lot number. The FDA has issued a nationwide recall of a ...

The U.S. Food and Drug Administration has listed a voluntary recall of a single lot of Xanax XR by a distributor of the ...

The Commissionerate of Food Safety and Drug Control, Rajasthan has issued a public alert after laboratory testing identified ...

Reflecting persistent drug quality concerns in India's pharmaceutical market, the Central Drugs Standard Control Organisation ...

Prioritising public health and patient safety, the Commissionerate of Food Safety and Drug Control, Rajasthan, has issued an ...

A radiation survivor and expert, an elderly returnee, and a wildlife researcher paint a picture of life 40 years later.

In a fresh drug safety alert underscoring continued regulatory vigilance, 48 batches of drugs, medical devices, and allied ...

A nationwide recall on a specific lot of Xanax was announced after the discovery of a quality issue related to the tablet breakdown process.