WhichRecall
Class IIReported 2025-05-07

Wegovy (semaglutide) injection, 2.4 mg/0.75 mL, 4 Single-Dose Prefilled Pens per Carton, For Subcutaneous Use Only, Rx Only, Single-Dose Only, Novo Nordisk Inc., Plainsboro, NJ 08536, Manufactured by: Novo Nordisk A/S, DK-2880, Bagsvaerd, Denmark, NDC 0169-4524-14.

Recalled by Cardinal Health Inc.

Reason for Recall

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

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More specifically, product was removed from refrigerated storage for an extended period of time and inappropriately released.

Recall Number
D-0393-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-04-09
Reported
2025-05-07
Distribution
NC, SC, VA
Code Info
Lot PZFDE06, Exp 08/31/2025
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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