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.
Reported: December 31, 2025 Initiated: December 12, 2025 #D-0242-2026
Product Description
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.
Reason for Recall
Presence of particulate matter: potential presence of metal particulates in the product.
Details
- Recalling Firm
- Merck Sharp & Dohme LLC
- Units Affected
- 845 kits
- Distribution
- Nationwide in the USA
- Location
- Wilson, NC
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Merck Sharp & Dohme LLC. Units affected: 845 kits.
Why was this product recalled? ▼
Presence of particulate matter: potential presence of metal particulates in the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 31, 2025. Severity: Moderate. Recall number: D-0242-2026.
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