Prometheus Laboratories Mercaptopurine Tablets, USP 50mg, a) 60-count bottle recall — FDA D-0249-2015
Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
Overview of recall records associated with Prometheus Laboratories Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
Failed USP Dissolution Test Requirements: The recalled lots do not meet the specification for dissolution.
This page summarizes recall records in which the official source identifies Prometheus Laboratories 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.