Apotex Scientific Duloxetine Delayed-Release Capsules, USP, 60 mg, 30-count bottles recall — FDA D-1436-2016
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Overview of recall records associated with Apotex Scientific, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 3.
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
Failed Dissolution Specification: Out of specification dissolution results when testing product stability.
This page summarizes recall records in which the official source identifies Apotex Scientific, Inc. 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.