Class IIReported 2025-04-16

Methocarbamol Injection USP 1,000 mg/10 mL (100 mg/mL), 10 mL Single Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Somerset, NJ 08873, NDC 70069-101-25 (immediate carton) and 70069-101-05 (5x10 mL carton)

Recalled by Somerset Therapeutics Private Limited

Reason for Recall

Lack of Assurance of Sterility: Media fill with bacterial contamination

Recall Number

D-0354-2025

Classification

Class II

Status

Ongoing

Category

drug

Initiated

2025-03-21

Reported

2025-04-16

Distribution

U.S. Nationwide

Code Info

NDC 70069-101-25; A240304, A240305, A240320, A240322, A240334, A240335, A240340, exp. date 05/2026; A240342, A240347, A240385, A240391, exp. date 06/2026; NDC 70069-101-05; A240326, exp. date 05/2026

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.