Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 25682-0001-01 recalled?

Soliris · 1 VIAL in 1 CARTON (25682-001-01) / 30 mL in 1 VIAL

Yes — this exact package was recalled

2 FDA recalls name the code 25682-0001-01 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.

Active ingredient
Eculizumab
Strength
ECULIZUMAB 300 mg/30mL
Form
Injection, Solution, Concentrate · Intravenous
Labeler
Alexion Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
25682-0001

Recalls naming this package

Class I · High risk

Soliris (eculizumab)

Presence of Particulate Matter: Product failed the appearance for the presence of visible particles under labeled storage condition.

Terminated Particulate / foreign matter Alexion Pharmaceuticals, Inc. NDC 25682-001-01 D-1512-2014
Class I · High risk

Soliris (eculizumab)

Presence of Particulate Matter: Failed the appearance test for the presence of visible particles.

Terminated Particulate / foreign matter Alexion Pharmaceuticals, Inc. NDC 25682-001-01 D-1049-2014

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.