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A batch of Xanax XR is being recalled nationwide after the producer discovered it could not launch the remedy within the physique as meant.
Viatris, Inc. initiated the voluntary recall for ALPRAZolam extended-release tablets, 3 mg, distributed in 60-count bottles below lot quantity 8177156 with an expiration date of Feb. 28, 2027, in keeping with the U.S. Meals and Drug Administration.
Xanax XR is a benzodiazepine used to deal with panic dysfunction and anxiousness in adults.
The problem was categorised as a Class II recall, which means it could trigger short-term or medically reversible well being results however is unlikely to end in critical hurt.
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A pharmacy tech pulls remedy from a shelf inside a pharmacy in Provo, Utah on Thursday, Aug. 7, 2025. (George Frey/Bloomberg through Getty Photographs / Getty Photographs)
“Failed dissolution specs” point out the tablets could not dissolve and launch the remedy on the meant price. As a result of Xanax XR is designed to launch progressively over time, any variation might have an effect on how the drug is delivered within the physique — and the way properly it really works.
The affected product was distributed nationwide in america, although the recall applies solely to the precise lot recognized. The FDA lists the recall as ongoing, with no termination date but introduced.
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On this picture illustration, the Viatris Inc. brand is seen displayed on a smartphone display screen. (Rafael Henrique/SOPA Photographs/LightRocket through Getty Photographs)
A spokesperson for Viatris informed FOX Enterprise the recall is restricted in scope and doesn’t pose a big danger to sufferers.
“The voluntary recall of Xanax XR within the U.S. is particular to 1 lot of 1 power (3mg) of the model product solely, and 51 bottles had been distributed to U.S. wholesalers between Aug. 27, 2024, and Could 29, 2025,” the spokesperson mentioned. “No different batches of the Xanax XR model product, or its generics, are impacted.”
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The spokesperson added that the majority sufferers within the U.S. are prescribed generic ALPRAZolam, which isn’t affected by the recall.
“The danger to the affected person related to this occasion is taken into account to be negligible. So far, no stories of hostile reactions related to this lot have been obtained,” the spokesperson mentioned.
Viatris mentioned the recall is being carried out on the retail degree, which means pharmacies and wholesalers have been instructed to return the affected product.
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“Sufferers don’t have to take any motion,” the spokesperson mentioned.
