Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Methocarbamol Injection USP 1 Recalled by Somerset Therapeutics Private Limited Due to Lack of Assurance of Sterility: Media fill with...

Date: March 21, 2025
Company: Somerset Therapeutics Private Limited
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Somerset Therapeutics Private Limited directly.

Affected Products

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)

Quantity: 506,080 vials

Why Was This Recalled?

Lack of Assurance of Sterility: Media fill with bacterial contamination

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Somerset Therapeutics Private Limited

Somerset Therapeutics Private Limited has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report