Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial recall — FDA D-0662-2026
Failed Impurities/Degradation Specifications
Overview of recall records associated with ONESOURCE SPECIALTY PHARMA LIMITED, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Failed Impurities/Degradation Specifications
This page summarizes recall records in which the official source identifies ONESOURCE SPECIALTY PHARMA LIMITED 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.