Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Triamcinolone Acetonide Injection Recalled for Glass Particulates

Agency Publication Date: October 5, 2023
Share:
Sign in to monitor this recall

Summary

Eugia US LLC is recalling 1,626 vials of Triamcinolone Acetonide Injectable Suspension, USP (400 mg per 10 mL). This recall was initiated because a piece of glass, measuring roughly 1 cm by 0.5 cm, was found inside a vial. This medication is typically used for intramuscular or intra-articular injections and should not be used if the product contains any visible particles.

Risk

The presence of glass particulates in an injectable medication poses a risk of local irritation, inflammation, or infection. If the glass fragment is injected, it could lead to more serious complications such as vascular damage or an embolism (a blockage in the blood vessels).

What You Should Do

  1. This recall affects Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), sold in 10 mL multiple dose vials (NDC 55150-385-01).
  2. Identify affected vials by checking for lot number 3TC22010 with an expiration date of 11/30/2024 printed on the label.
  3. Stop using the recalled product immediately.
  4. Contact the manufacturer, Eugia US LLC, or your medical distributor to arrange for the return of the affected vials.
  5. If you have health concerns regarding a previous injection of this product, contact your healthcare provider or pharmacist.
  6. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Triamcinolone Acetonide Injectable Suspension, USP
Variants: 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, Intramuscular or Intra-articular use
Lot Numbers:
3TC22010 (Exp 11/30/2024)
NDC:
55150-385-01

Manufactured in India for Auromedics Pharma LLC. Lot quantity: 1,626 vials.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93128
Status: Active
Manufacturer: Eugia US LLC
Sold By: Auromedics Pharma LLC; Medical wholesalers; Hospitals; Clinics
Manufactured In: India
Units Affected: 1,626 vials
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 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.