HIGH

Novo Nordisk Recalls Wegovy Injection Due to Contamination Risk

Novo Nordisk recalled Wegovy (semaglutide) Injection on December 19, 2025, due to hair found in a prefilled syringe. The recall affects products distributed nationwide in the United States. Consumers should stop using the product immediately and contact their healthcare provider.

Quick Facts at a Glance

Recall Date
December 19, 2025
Hazard Level
HIGH
Brands
Wegovy, Novo Nordisk
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Novo Nordisk Inc. or your healthcare provider for guidance. Notification method: Letter

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Product Details

Wegovy (semaglutide) Injection, 1 mg/0.5 mL, includes four single-dose prefilled pens. The affected lots are Lot #: RZFYK06 and RZFYA53, with an expiration date of March 31, 2027. The product is manufactured by Novo Nordisk A/S, Bagsvaerd, Denmark, and distributed in the U.S.

The Hazard

The recall stems from the discovery of hair in a prefilled syringe, posing a contamination risk. This issue falls under Class II, indicating a potential for serious health consequences.

Reported Incidents

There have been no reported incidents of injury or adverse effects linked to this contamination at this time.

What to Do

Consumers and healthcare providers should stop using Wegovy immediately. Contact Novo Nordisk or your healthcare provider for further guidance. Notification will be sent via letter.

Contact Information

For more information, contact Novo Nordisk Inc. at their Plainsboro, NJ office or visit their website.

Key Facts

  • Recall date: December 19, 2025
  • High hazard level
  • Class II recall
  • No injuries reported

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot #: RZFYK06
RZFYA53
UPC Codes
0169-4404
0169-4525
0169-4505
+16 more
Affected States
ALL
Report Date
January 7, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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