US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Dec 12, 2025 (9 months ago)

Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was 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

Recalling firm
Merck Sharp & Dohme LLC
NDC code
0006-3066-03
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0241-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Aprepitant recalls

See all