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Serious recall: Injury is possible or has been reported. Take action promptly.

Amerisource Health Services LLC 2024-07-17 Health serious FDA
Health · FDA · Recall #FDA-D-0590-2024

buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets… Recall

Issued July 17, 2024 · Amerisource Health Services LLC

In July 2024, Amerisource Health Services LLC recalled the buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Failed Dissolution Specifications; the product is dissolving faster than the specified limits.

What you should do

  1. 1 Stop using buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Amerisource Health Services LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Amerisource Health Services LLC
Category
Health
Recall date
July 17, 2024
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0590-2024
Made in
United States
Issuing agency
FDA

In context

  • Amerisource Health Services LLC has 20 recalls in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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