US Drug Recall Register
Class I · High risk Terminated Initiated Sep 17, 2024 (2 years ago)

Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle, Rx only, Distributed by…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.

What was recalled

Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, NDC # 69452-252-87.

Recalling firm
Bionpharma Inc.
NDC code
69452-252-87
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0012-2025

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 Atovaquone recalls

See all