The Recall Desk
HighFDA (Drugs)·D-0244-2026·Announced 2026-01-07

Wegovy 0.5 mg pens recalled after hair was found in a syringe

Novo Nordisk is recalling Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL prefilled pens, over the presence of particulate matter after hair was found in a prefilled syringe.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Scored 3 under the risk-of-harm criterion: particulate matter found inside an injectable product is a stated contaminant, and no injuries are reported.

Plain-English summary

Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, supplied as 4 single-dose prefilled pens, manufactured by Novo Nordisk A/S of Bagsvaerd, Denmark, under NDC 0169-4505-14, is being recalled.

The reason given in the enforcement record is the presence of particulate matter: hair was found in a prefilled syringe.

The recall covers lots RZFHD52 and RZFHW93, both with an expiry date of 10/31/2026. The record does not state a quantity. Distribution was nationwide within the United States. The FDA has classified the action as Class II.

Patients should not stop using a prescribed medicine without speaking to their prescriber or pharmacist, who can confirm whether a specific pen is affected and arrange a replacement.

The recalled product

Product
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
Manufacturer
Novo Nordisk Inc.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot #: RZFHD52
  • RZFHW93
  • Exp Date 10/31/2026

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 2 recalled by Novo Nordisk Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →