Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension Recalled by Merck Sharp & Dohme LLC Due to Presence of particulate matter: potential presence of metal...

Date: December 12, 2025
Company: Merck Sharp & Dohme LLC
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Merck Sharp & Dohme LLC directly.

Affected Products

Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufactured for: Merck Sharp & Doohme LLC, Rahway, NJ 07056 USA, Manufactured by: N.V. Organon, 5349 AB Oss, The Netherlands, a subsidiary of Organon & Co., Jersey City, NJ 07302, USA NDC 0085-2224-02.

Quantity: 845 kits

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Merck Sharp & Dohme LLC

Merck Sharp & Dohme LLC has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report