Overview of recall records associated with Actavis South Atlantic LLC, including dates, categories and classifications where available.
Classification mix: Class III: 2.
Failed Dissolution Specifications: This recall is an extension of the recall initiated on 07/31/2013 for Bupropion HCl Extended-Release Tablets (XL) 300 mg, because another lot was shown to…
Failed USP Dissolution Test Requirements: Out-of-specification dissolution results at the 8 hour stability testing point.
This page summarizes recall records in which the official source identifies Actavis South Atlantic LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
