Methocarbamol Injection USP 1,000 mg/10 mL (100 mg/mL), 10 mL Single Dose Vial recall — FDA D-0354-2025
Lack of Assurance of Sterility: Media fill with bacterial contamination
Overview of recall records associated with Somerset Therapeutics Private Limited, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Lack of Assurance of Sterility: Media fill with bacterial contamination
Lack of Assurance of Sterility: Media fill with bacterial contamination
This page summarizes recall records in which the official source identifies Somerset Therapeutics Private 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.