HIGH

Novo Nordisk Issues Recall of Wegovy Injection Due to Contamination

Novo Nordisk recalled Wegovy (semaglutide) injections on December 19, 2025, after discovering hair in prefilled syringes. The contamination poses a serious hazard to consumers. The recall affects all units distributed nationwide.

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

The recall involves Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, packaged as 4 Single-Dose Prefilled Pens. The affected lot numbers are RZFHD52 and RZFHW93, with an expiration date of October 31, 2026. The product was distributed throughout the United States.

The Hazard

The recalled product contains particulate matter, specifically hair, in the prefilled syringe. This contamination can lead to serious health risks if injected.

Reported Incidents

No specific injuries or incidents have been reported related to this recall. The presence of hair in a medication delivery system raises significant health concerns.

What to Do

Consumers and healthcare providers should stop using Wegovy immediately. Contact Novo Nordisk Inc. or your healthcare provider for further guidance.

Contact Information

For assistance, consumers can reach Novo Nordisk Inc. at their Plainsboro, NJ office or visit the FDA's website for more information.

Key Facts

  • Recall date: December 19, 2025
  • Reported contamination: Hair found in prefilled syringes
  • Health classification: Class II
  • Manufactured by: Novo Nordisk A/S, Denmark

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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 #: RZFHD52
RZFHW93
Exp Date 10/31/2026
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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