Class I · High risk
Veklury (remdesivir)
Presence of Particulate Matter: Presence of glass particle.
National Drug Code
Is NDC 61958-2901-02 recalled?
Veklury · 1 VIAL, SINGLE-DOSE in 1 CARTON (61958-2901-2) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
2 FDA recalls name the code 61958-2901-02 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
- remdesivir
- Strength
- REMDESIVIR 100 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intravenous
- Labeler
- Gilead Sciences, Inc.
- Type
- Human Prescription Drug
- Product code
- 61958-2901
Recalls naming this package
Class I · High risk
Veklury (remdesivir)
Presence of Particulate Matter: investigation into a customer complaint confirmed the presence of glass particulates.
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
- 61958-0101 See recall 1
- 61958-0602 Emtriva 1
- 61958-0701 Truvada 1
- 61958-0901 Cayston 1
- 61958-1003 See recall 1
- 61958-2401 Vosevi 1
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