Novo Nordisk Inc.: Drug Recall
Recall #D-0245-2026 · 12/19/2025
Class II: Risk
Recall Details
- Recall Number
- D-0245-2026
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Novo Nordisk Inc.
- Status
- Ongoing
- Date Initiated
- 12/19/2025
- Location
- Plainsboro, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Reason for Recall
Presence of Particulate Matter: Hair was found in a prefilled syringe
Product Description
Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4501-14
Distribution Pattern
Nationwide within the United States.
Other Recalls by Novo Nordisk Inc.
- Class II: Risk 12/19/2025
- Class II: Risk 03/22/2021
- Class I: Dangerous 03/22/2021
- Class II: Risk 03/22/2021
- Class II: Risk 03/22/2021
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.