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Akorn Recalls Various Drug Products Due to Company Shutdown

Akorn has initiated a voluntary recall of various within-expiry drug products as the company has shut down operations and is unable to assure the quality of the products.

The recalled products were distributed nationwide to wholesalers, retailers, manufacturers, medical facilities, and repackagers and via the Internet to consumers. The discontinuation of the Company’s Quality program means that it is unable to support or guarantee that the medications will meet all intended specifications through the labeled shelf life of the product. Improve Testosterone

Akorn Recalls Various Drug Products Due to Company Shutdown

All NDCs and Lots of the following Akorn products have been recalled:

Further distribution or use of these recalled products should be discontinued immediately. To date, the Company has not received any reports of adverse events related to this recall.

Adverse events or quality issues should be reported to the FDA’s MedWatch Adverse Event Reporting program. Consumers with questions regarding this recall can contact Akorn at (800) 932-5676.

Akorn issues voluntary nationwide recall of various human and animal drug products within expiry due to company shutdown. News release. Akorn. Accessed April 26, 2023. https://www.prnewswire.com/news-releases/akorn-issues-voluntary-nationwide-recall-of-various-human-and-animal-drug-products-within-expiry-due-to-company-shutdown-301808215.html.

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Akorn Recalls Various Drug Products Due to Company Shutdown

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