FDAFDA · Food and drugs·Recall number D-0354-2025
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)
Published April 16, 2025 · Recall initiated: March 21, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Media fill with bacterial contamination
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- METHOCARBAMOL
- Manufacturer
- Somerset Therapeutics Private Limited
- Distributor
- U.S. Nationwide
- UPC
- 0370069101018
- Lot
- 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
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- India
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