The company voluntarily initiated the recall after a batch of bottles containing 60 3-mg tablets of the drug failed dissolution specifications. Aurobindo Pharma USA, Inc., on behalf of AuroHealth, is voluntarily recalling one lot. Contact 1-866-850-2876 (Option 2) Recall being handled … 3 mg Xanax XR tablets (60-count bottles) were first recalled on March 17, with the recall expanded nationwide on April 15 after the medication … The FDA announced a voluntary recall of select lots of Xanax. · The impacted lots may dissolve too quickly or not fast enough in the body. Xanax XR (alprazolam) extended release 00009006807 Failed Dissolution Specifications. If you have questions about this recall, Aurobindo Pharma … The recalled pills were distributed in 60-pill bottles between August 2024 and May 2025, according to Viatris. Bottles of the affected pills are … The pharmacist said they hadn\’t received any other ppl asking but she did say she doesn\’t recall getting it from this mfg in a long time. 11/19/24 Endo USA, Inc. Clonazepam Orally Disintegrating Tablets, USP (C-IV) 60 count carton presentation. 11/18/24 Aurobindo Pharma USA, Inc. Lot number 8177156 was recalled, with bottles containing 60, 3mg extended-release tablets. The expiration date for the bottles was Feb. 28, 2027 … AuroHealth is voluntarily recalling one lot (refer table below) of Healthy Living Migraine Relief, Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg … The FDA is investigating and recalling select bottles of Xanax after the pills failed to dissolve properly during testing. The generic drug alprazolam is unstable, varies in effectiveness and sometimes doesn\’t seem to have any effect at all. ANI Pharmaceuticals Inc is recalling more than 500,000 bottles of alprazolam tablets because of deviations from Current Good Manufacturing … The FDA issued a voluntary recall of Xanax XR manufactured by Viatris due to failure to meet dissolution specifications, which could make … The recalled pills were distributed in 60-pill bottles between August 2024 and May 2025, according to Viatris. Bottles of the affected pills are … The recalled medication includes 3-milligram pills of brand-name Xanax XR in bottles of 60 tablets. These are the “extended release” version of … The voluntary recall of Xanax XR in the U.S. is specific to one lot of one strength (3mg) of the brand product only, and no other batches of the … A nationwide recall has been issued for a batch of Xanax XR after the manufacturer found the medication may not release as intended. As for Aurobindo, the company recalled a total of 96 bottles of rufinamide tablets for treating seizure disorders. The company\’s recall covers … According to the FDA, the voluntary recall involves Xanax XR extended-release tablets distributed across the U.S. between Aug. 27, 2024, and May … According to the notice, the drug was recalled because it \“failed dissolution specifications.\“ This means the drug may have failed quality … Xanax recall: What to know. The recalled bottles are from Lot #8177156, with an expiration date of Feb. 28, 2027, according to the FDA notice … According to WKYT, 3 mg Xanax XR tablets (60-count bottles) were first recalled on March 17, with the recall expanded nationwide on April 15 … On March 17, the distributor recalled 3-milligram tablets of Xanax XR, sold in 60-tablet bottles. On April 15, the pills were recalled … The recalled bottles of Xanax were distributed nationwide between Aug. 27, 2024, and May 29, 2025, according to the California State Board of … The recall affects only one lot of 3 mg Xanax tablets provided in 60-tablet bottles, though the FDA has not indicated how many pills or bottles … The specific product included in the recall was: Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed … The recall is for 3 mg Xanax XR, the brand name for alprazolam. Affected items are in 60 tablet bottles. The recall was voluntary and initiated …