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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Wegovy Injection Recalled for Potential Temperature Exposure

Agency Publication Date: April 28, 2025
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Summary

Cardinal Health Inc. has recalled 48 cartons of Wegovy (semaglutide) injection, 2.4 mg/0.75 mL, after the medication was potentially exposed to temperatures outside of its required storage range. This exposure occurred due to a shipping error at a distribution center, where the refrigerated medication was removed from storage for an extended period and inappropriately released. Each recalled carton contains four single-dose prefilled pens.

Risk

Exposure to temperatures outside of the manufacturer's labeled storage conditions can compromise the safety and effectiveness of the medication, which may lead to inadequate treatment for patients using the injection.

What You Should Do

  1. This recall involves Wegovy (semaglutide) injection, 2.4 mg/0.75 mL, sold in cartons of four single-dose prefilled pens under NDC 0169-4524-14, featuring lot number PZFDE06 and an expiration date of 08/31/2025.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact Cardinal Health Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional assistance.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Wegovy (semaglutide) injection (2.4 mg/0.75 mL)
Variants: 2.4 mg/0.75 mL, Single-Dose Prefilled Pen, 4 Pens per Carton
Lot Numbers:
PZFDE06 (Exp 08/31/2025)
NDC:
0169-4524-14

Quantity: 48 Cartons. Manufactured by Novo Nordisk A/S.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96637
Status: Active
Manufacturer: Cardinal Health Inc.
Sold By: Cardinal Health Inc. Distribution Centers; Pharmacies in North Carolina; Pharmacies in South Carolina; Pharmacies in Virginia
Manufactured In: Denmark, United States
Units Affected: 48 Cartons
Distributed To: North Carolina, South Carolina, Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.