Eugia recalls Methocarbamol injection with particulate matter risk

Take action

Contact the company & request your remedy

Recalling firmEugia US LLC279 Princeton Hightstown Rd, N/A · East Windsor, NJ 08520-1401

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Eugia US LLC is recalling Methocarbamol injection vials that may contain particulate matter. This could cause serious injury if injected into the body. The recall affects specific vials manufactured in India with lot number 3MC23011.

Why it’s dangerous

Particulate matter in the injection can cause blockages or injuries when injected. This risk is serious because it could lead to complications like infections or tissue damage.

Who’s affected

Prescription users in the US who received Methocarbamol injection vials with lot number 3MC23011 from Eugia US LLC. Healthcare providers and patients using this medication are most at risk.

How to tell if you have this one

Check for vials labeled 'Methocarbamol Injection, USP 1000mg/10mL (100mg/mL), 10 mL Single-Dose Vial' packed 25 per carton. The lot number 3MC23011 was manufactured in India with expiration date 11/30/2026.

Brand
Eugia
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Vial Details
Look for the lot number 3MC23011 on the vial packaging to confirm if it is affected.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a potential risk of particulate matter, so it is not safe to use the affected vials.

What should I do if I have the affected vial?

The recall does not specify a remedy, so contact Eugia US LLC for guidance.

How can I confirm if my vial is affected?

Check the lot number on the vial packaging; affected vials have lot number 3MC23011.

Take action

Contact Eugia

We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0440-2024 — Eugia Eugia

Hello,

I own a Eugia that is covered by recall D-0440-2024 from Eugia.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0440-2024 (February 15, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0440-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Eugia US LLC recalls Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd.

Recall notice