Quick Facts at a Glance
- Recall Date
- December 12, 2025
- Hazard Level
- HIGH
- Brands
- EMEND, Merck Sharp & Dohme LLC
- 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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- EMEND, Merck Sharp & Dohme LLC
- Product type
- Prescription Medication
- Model numbers
- Lot #: Z014503, Exp 11/15/2027
- UPC codes
- 0006-0461, 0006-0462, 0006-3862, 0006-0464, 0006-3066, 0006-0461-02, 0006-0461-01, 0006-0461-06 +7 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 12, 2025
Reported by FDA DRUG
December 31, 2025
RecallRadar source check
January 7, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Presence of particulate matter: potential presence of metal particulates in the product.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Merck Sharp & Dohme LLC or your healthcare provider for guidance. Notification method: Letter
About This Product
Merck Emend (aprepitant) is a prescription medication used to prevent nausea and vomiting caused by chemotherapy. Patients typically use it as part of a treatment regimen for cancer.
Why This Is Dangerous
The recall is due to the potential presence of metal particulates in the oral suspension, which can pose serious health risks if ingested. Consumers may experience adverse health effects from consuming contaminated products.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should stop using the medication immediately to avoid potential health risks. The recall may cause inconvenience for patients needing nausea control during chemotherapy.
Practical Guidance
How to identify if yours is affected
- Check the lot number on your product to see if it is Z014503.
- Verify the expiration date; affected products expire on November 15, 2027.
- If unsure, consult your healthcare provider.
Where to find product info
The lot number and expiration date are usually found on the packaging or label of the medication.
What timeline to expect
Expect refund processing to take approximately 4 to 6 weeks after your request is submitted.
If the manufacturer is unresponsive
- Contact Merck Sharp & Dohme LLC support directly.
- Document all correspondence and attempts to resolve the issue.
How to prevent similar issues
- When purchasing prescription medications, always check for recalls and safety alerts.
- Consult healthcare providers about alternative medications if recalls occur.
- Stay informed about product safety news through reliable health sources.
Documentation advice
Keep a record of purchase receipts and any correspondence regarding the recall for future reference.
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Product Details
The recalled product is Merck Emend (aprepitant) for oral suspension, 125 mg, in a single-dose kit. The lot number is Z014503, and it expires on November 15, 2027. The product was distributed nationwide in the USA.
Key Facts
- Recalled product: Emend (aprepitant) for oral suspension
- Lot #: Z014503, Expiration: 11/15/2027
- Recall date: December 12, 2025
- Potential metal contamination hazard
- Stop use immediately and contact healthcare provider
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Safety Guide
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