Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 50242-0078-55 recalled?

Susvimo · 1 VIAL in 1 CARTON (50242-078-55) / 1 mL in 1 VIAL

Yes — this exact package was recalled

1 FDA recall names the code 50242-0078-55 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
Ranibizumab
Strength
RANIBIZUMAB 100 mg/mL
Form
Injection, Solution · Intravitreal
Labeler
Genentech, Inc.
Type
Human Prescription Drug
Product code
50242-0078

Recalls naming this package

Class III ยท Low risk

Susvimo (ranibizumab injection)

Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.

Terminated Packaging defect Genentech Inc NDC 50242-078-55 D-0025-2023

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