Bottles of anxiety medication Xanax recalled nationwide – NBC Chicago
Bottles of a preferred medication used to deal with anxiety and panic issues are being recalled nationwide, in line with a report from the Food and Drug Administration.
One lot of Xanax, one of the most widely prescribed benzodiazepineswas recalled March 17 by pharmaceutical firm Viatris as a result of the drug failed to satisfy dissolution specs. According to the FDA, the voluntary recall was listed as a “Class II” recall, which suggests non permanent, hostile well being penalties are doable.
According to well being officers, medicine that do not meet “dissolution specifications” may imply the capsules aren’t as efficient, or that they do not launch the right dosage.
Lot quantity 8177156 was recalled, with bottles containing 60, 3mg extended-release tablets. The expiration date for the bottles was Feb. 28, 2027, the FDA stated.
The capsules have been distributed nationwide between Aug. 27, 2024, and May 29, 2025, the California State Board of Pharmacy he stated. It wasn’t instantly clear what number of bottles have been recalled.
Vitaris Inc. didn’t instantly reply to NBC 5’s request for remark.
