Overview of recall records associated with Forest Pharmaceuticals Inc., including dates, categories and classifications where available.
Classification mix: Class III: 2, Class II: 1.
Failed Dissolution Specifications: One lot of product is being voluntarily recalled because dissolution test results failed to meet specification throughout the product's shelf life.
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
This page summarizes recall records in which the official source identifies Forest Pharmaceuticals 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.
