HIGHFDA DRUG

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.

Official notice
WegovyNovo NordiskHealth & Personal CareDrugs & MedicationsLot #: RZFHD52RZFHW93Exp Date 10/31/2026

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
December 19, 2025
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Wegovy, Novo Nordisk
Product type
Injection
Model numbers
Lot #: RZFHD52, RZFHW93, Exp Date 10/31/2026
UPC codes
0169-4404, 0169-4525, 0169-4505, 0169-4501, 0169-4517, 0169-4524, 0169-4415, 0169-4409 +11 more
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 19, 2025

  2. Reported by FDA DRUG

    January 7, 2026

  3. RecallRadar source check

    January 14, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Wegovy is a prescription medication used for weight management in adults. It is administered via injection and helps regulate appetite and caloric intake.

Why This Is Dangerous

The presence of hair in the syringe poses a contamination risk that could lead to infections or other health complications if injected.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers are urged to stop using this product to avoid serious health risks associated with contamination.

Practical Guidance

How to identify if yours is affected

  1. Check the lot number on your Wegovy injection pens.
  2. Verify if the lot number is RZFHD52 or RZFHW93.
  3. Confirm the expiration date is October 31, 2026.

Where to find product info

The lot number and expiration date can typically be found on the product packaging.

What timeline to expect

Expect a refund or replacement within 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Follow up with Novo Nordisk if you do not receive a response within a week.
  • Document all communications with the company.

How to prevent similar issues

  • Always inspect the packaging and syringe before use.
  • Be aware of recalls related to medications and injectables.
  • Consult your healthcare provider for alternatives if recalls occur.

Documentation advice

Keep a record of your purchase, any communications with Novo Nordisk, and photographs of the product for reference.

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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.

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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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