Recall Ledger

Merck Emend recall (Merck Sharp & Dohme LLC)

DrugClass IIOngoing

Summary: Merck Sharp & Dohme LLC is recalling Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03. Reason: Presence of particulate matter: potential presence of metal particulates in the product.

What is being recalled

Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03

Why

Presence of particulate matter: potential presence of metal particulates in the product.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

Nationwide in the USA

How to tell if yours is affected

Lot #: Z014503, Exp 11/15/2027

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0241-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedDecember 12, 2025
ReportedDecember 31, 2025
CompanyMerck Sharp & Dohme LLC
Company locationWilson, NC, United States
Initiated byVoluntary: Firm initiated
Quantity3 - single dose kits

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