Class I · High risk
VPRIV¿ (velaglucerase alfa for injection)
Presence of Particulate Matter; Particulates identified as stainless steel and barium sulfate.
National Drug Code
Is NDC 54092-0701-04 recalled?
Vpriv · 1 VIAL, GLASS in 1 BOX (54092-701-04) / 4 mL in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 54092-0701-04 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.
- Active ingredient
- velaglucerase alfa
- Strength
- VELAGLUCERASE ALFA 2.5 mg/mL
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Takeda Pharmaceuticals America, Inc.
- Type
- Human Prescription Drug
- Product code
- 54092-0701
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
- 54092-0189 Pentasa 2
- 54092-0606 See recall 2
- 54092-0191 Pentasa 1
- 54092-0252 Fosrenol 1
- 54092-0552 See recall 1
- 54092-0553 See recall 1
Free recall alerts
Know the day your medication is recalled
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