Class II · Moderate risk
Triamcinolone Acetonide Injectable Suspension
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.
National Drug Code
Is NDC 55150-0385-01 recalled?
Triamcinolone Acetonide · 1 VIAL, MULTI-DOSE in 1 CARTON (55150-385-01) / 10 mL in 1 VIAL, MULTI-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 55150-0385-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Triamcinolone Acetonide
- Strength
- TRIAMCINOLONE ACETONIDE 40 mg/mL
- Form
- Injection, Suspension · Intra-Articular, Intramuscular, Soft Tissue
- Labeler
- Eugia US LLC
- Type
- Human Prescription Drug
- Product code
- 55150-0385
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 55150-0120 Piperacillin and Tazobactam 2
- 55150-0183 Nicardipine Hydrochloride 2
- 55150-0202 Pantoprazole Sodium 2
- 55150-0242 Linezolid 2
- 55150-0243 Levofloxacin 2
- 55150-0306 Progesterone 2
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