FDAFDA · Food and drugs·Recall number D-0041-2024
Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For Intramuscular or Intra-articular use only, Shake Well, Not for IV/ID, intraocular, epidural, or intrathecal use, Mfd. in India for Auromedics Pharma LLC., E Windsor, NJ, 08520, NDC 55150-385-01.
Published October 11, 2023 · Recall initiated: September 28, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated
Recall details
- Brand
- TRIAMCINOLONE ACETONIDE
- Manufacturer
- Eugia US LLC
- Distributor
- Nationwide in the USA
- UPC
- 0355150384013
- Lot
- Lot #: 3TC22010, Exp 11/30/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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