Eugia US LLC recalls Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For
Eugia US LLC recalls 400 mg per 10 mL Triamcinolone Acetonide Injectable Suspension vials due to glass particles found in some units. This may cause injury during injection. Affected vials have NDC 55150-385-01 and were manufactured in India for Auromedics Pharma LLC.
Use caution until it’s fixed
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Contact the company & request your remedy
What happened, in plain English
Eugia US LLC is recalling triamcinolone injectable vials after finding glass particles in some units. This could cause injury if injected, so affected users should stop using the product. Read more at govinfonow.com/recall/33093-eugia-triamcinolone-vial-recall-glass-particles-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/33093-eugia-triamcinolone-vial-recall-glass-particles-risk · Updated September 23, 2026 · FDA enforcement record: FDA #D-0041-2024
Cite this page
“Eugia Triamcinolone Vial Recall: Glass Particles Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/33093-eugia-triamcinolone-vial-recall-glass-particles-risk. Based on FDA recall #D-0041-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0041-2024%22&limit=1).
Why it’s dangerous
Glass particles found in the vial could cause injury when injected into the body. The particles are visible as a 1 cm x 0.5 cm piece of glass inside the vial.
Who’s affected
People with prescriptions for this injectable steroid medication are affected. Those using the vial for injections are most at risk.
How to tell if you have this one
Check for vials labeled 'Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial'. The NDC number is 55150-385-01 and was manufactured in India for Auromedics Pharma LLC.
- Brand
Eugia- Category
Drug
What to do — step by step
Check Vial Label
Look for the NDC number 55150-385-01 on the vial label.
Stop Using Vial
If you have the recalled vial, do not use it for injections.
Questions people ask
Is this product safe to use?
No, the vial contains glass particles that could cause injury during injection.
How can I tell if I have the recalled vial?
Check for the NDC number 55150-385-01 on the vial label.
What should I do if I have the recalled vial?
Do not use the vial for injections. Contact your doctor for alternative options.
Contact Eugia
We’ve drafted a message you can send Eugia to request your refund or repair — edit it as you like.
Subject: Recall D-0041-2024 — Eugia Eugia Hello, I own a Eugia that is covered by recall D-0041-2024 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.
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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-0041-2024 (September 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0041-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.