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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

Merck Emend and Noxafil Oral Suspensions Recalled for Metal Particulates

Agency Publication Date: December 23, 2025
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Summary

Merck Sharp & Dohme LLC is recalling 848 kits of Emend (aprepitant) and Noxafil Powdermix (posaconazole) oral suspensions because they may contain metal particles. This voluntary recall affects 3 kits of Emend and 845 kits of Noxafil distributed nationwide. Consumers who have these medications should check their lot numbers and contact their healthcare provider or pharmacist.

Risk

The presence of metal particulates in an oral medication poses a potential risk of irritation or injury to the digestive tract. If the particles are small enough to be absorbed or if the product is administered through a feeding tube, they could cause more serious internal complications or mechanical blockages.

What You Should Do

  1. Check your medication packaging for the following product names and lot numbers: Emend (aprepitant) lot Z014503 (Exp 11/15/2027) or Noxafil Powdermix (posaconazole) lots Z012339, Z010344, Z009908, or Z009909 with expiration date 12-31-2026.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

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: Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit
Variants: 125 mg, Single-Dose Kit
Lot Numbers:
Z014503 (Exp 11/15/2027)
NDC:
0006-3066-03

Manufactured by Novo Nordisk Production Ireland Limited

Product: Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg
Variants: 300 mg, 8 packets per carton
Lot Numbers:
Z012339 (Exp 12-31-2026)
Z010344 (Exp 12-31-2026)
Z009908 (Exp 12-31-2026)
Z009909 (Exp 12-31-2026)
NDC:
0085-2224-02

Manufactured by N.V. Organon

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98113
Status: Active
Manufacturer: Merck Sharp & Dohme LLC
Sold By: Pharmacies
Manufactured In: United States, Ireland, Netherlands
Units Affected: 2 products (3 - single dose kits; 845 kits)
Distributed To: Nationwide

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.