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

FDA Recall #D-0241-2026 — Class II — December 12, 2025

Recall #D-0241-2026 Date: December 12, 2025 Classification: Class II Status: Ongoing

Product Description

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 for Recall

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

Recalling Firm

Merck Sharp & Dohme LLC — Wilson, NC

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

3 - single dose kits

Distribution

Nationwide in the USA

Code Information

Lot #: Z014503, Exp 11/15/2027

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated