Recall Ledger

Wegovy recall (Novo Nordisk Inc.)

DrugClass IIOngoing

Summary: Novo Nordisk Inc. is recalling 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. Reason: Presence of Particulate Matter: Hair was found in a prefilled syringe.

What is being recalled

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

Why

Presence of Particulate Matter: Hair was found in a prefilled syringe

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

Nationwide within the United States.

How to tell if yours is affected

Lot #: RZFYK06, RZFYA53; Exp Date 3/31/2027

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0245-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedDecember 19, 2025
ReportedJanuary 7, 2026
CompanyNovo Nordisk Inc.
Company locationPlainsboro, NJ, United States
Initiated byVoluntary: Firm initiated
QuantityN/A

More recalls from Novo Nordisk Inc. · all drug recalls · recalls from December 2025

Official FDA record