D-0244-2026 Class II Ongoing
FDA drug recall D-0244-2026 was initiated by Novo Nordisk Inc. on Dec 19, 2025 and is designated Class II. Reason for recall: Presence of Particulate Matter: Hair was found in a prefilled syringe The recall status is ongoing.
Recall Details
- Product Type
- Drugs
- Report Date
- Jan 7, 2026
- Initiation Date
- Dec 19, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
Wegovy (semaglutide) Injection, 0.5 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 0169-4505-14
Reason for Recall
Presence of Particulate Matter: Hair was found in a prefilled syringe
Distribution Pattern
Nationwide within the United States.
Code Information
Lot #: RZFHD52, RZFHW93; Exp Date 10/31/2026
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0244-2026
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026