Drug recall D-0041-2024
Product
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.
Reason for recall
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.
Lots and codes
Lot #: 3TC22010, Exp 11/30/2024
Recall details
- Recalling firm
- Eugia US LLC, East Windsor, NJ
- Quantity
- 1,626 vials
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- September 28, 2023
Related products
- Triamcinolone Acetonide – drug information
- NDC 55150-384 Triamcinolone Acetonide · Triamcinolone Acetonide 40 mg/mL · Eugia US LLC
- NDC 55150-385 Triamcinolone Acetonide · Triamcinolone Acetonide 40 mg/mL · Eugia US LLC