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Class II · ModerateActive recall

Wegovy

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot PZFDE06, Exp 08/31/2025
Where it was soldNC, SC, VA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byNovo Nordisk A/S, DK-2880, Bagsvaerd, Denmark
Brand nameWEGOVY
Generic nameSEMAGLUTIDE
Active ingredient(s)SEMAGLUTIDE
Distributed by / forCardinal Health Inc.
NDC0169-4524-14
Show the full FDA record
Full product labelWegovy (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.
Recalling firmCardinal Health Inc.
DistributionNC, SC, VA
Quantity48 Cartons
Recall initiated2025-04-09
Report date2025-05-07
Recall completed
Recall numberD-0393-2025
ClassificationClass II
FDA statusOngoing
Origin on fileDublin OH United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.