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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

Methocarbamol Injection Recalled for Presence of Particulate Matter

Agency Publication Date: April 8, 2024
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Summary

Eugia US LLC has recalled 1,552 cartons of Methocarbamol Injection, USP 1000mg/10mL (100mg/mL) due to the presence of particulate matter in the vials. Methocarbamol is a prescription medication used to treat muscle spasms and is administered by injection in clinical settings. The recall affects 10 mL single-dose vials packaged 25 per carton.

Risk

Injecting a drug containing particulate matter can cause serious health complications, such as blood vessel blockages, inflammation, or allergic reactions. These particles can travel through the bloodstream to the lungs or other organs, posing a risk of severe injury.

What You Should Do

  1. This recall affects Methocarbamol Injection, USP (1000mg/10mL) sold in 10 mL single-dose vials with NDC 55150-223-10, packaged 25 vials per carton.
  2. Check the medication label for lot number 3MC23011 with an expiration date of 11/30/2026.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer-coordinated return

How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial
Variants: 1000mg/10mL, 100mg/mL, Single-Dose Vial
UPC Codes:
355150223107
Lot Numbers:
3MC23011 (Exp 11/30/2026)
NDC:
55150-223-10

Packed 25 vials per carton; quantity affected: 1,552 10ml x 25/carton

Product Images

Product label: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial); NDC 55150-223-10

Product label: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial); NDC 55150-223-10

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94025
Status: Active
Manufacturer: Eugia US LLC
Sold By: Wholesalers; Hospitals; Medical facilities; Distributors
Manufactured In: India
Units Affected: 1,552 10ml x 25/carton
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.