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

Is NDC 0169-4524-14 recalled?

Wegovy · 4 SYRINGE, PLASTIC in 1 CARTON (0169-4524-14) / .75 mL in 1 SYRINGE, PLASTIC (0169-4524-01)

Yes — this exact package was recalled

1 FDA recall names the code 0169-4524-14 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.

1 of these recalls is still ongoing.

Active ingredient
semaglutide
Strength
SEMAGLUTIDE 2.4 mg/.75mL
Form
Injection, Solution · Subcutaneous
Labeler
Novo Nordisk Pharmaceutical Industries, LP
Type
Human Prescription Drug
Product code
0169-4524

Recalls naming this package

Class II ยท Moderate risk

Wegovy (semaglutide)

Temperature abuse: Wegovy product was potentially exposed to temperatures outside of the products labeled storage conditions due to a shipping error involving a Cardinal Health distribution center. More specifically, product was removed from refrigerated storage for an extended period of time and inappropriately released.

Ongoing Temperature excursion Cardinal Health Inc. NDC 0169-4524-14 D-0393-2025

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