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

Is NDC 50242-0175-05 recalled?

Evrysdi

Yes — this exact package was recalled

1 FDA recall names the code 50242-0175-05 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
Risdiplam
Strength
RISDIPLAM .75 mg/mL
Form
Powder, for Solution · Oral
Labeler
Genentech, Inc.
Type
Human Prescription Drug
Product code
50242-0175

Recalls naming this package

Class III ยท Low risk

Evrysdi (risdiplam)

Defective Container: complaints received regarding some incorrect press-in-bottle-adapters (PIBA), the incorrect PIBAs have a female instead of male fit so they cannot be used in combination with co-packed syringes.

Terminated Packaging defect Genentech Inc D-0357-2021

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