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Fusion Pharmaceuticals, LLC

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20141
20151
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FDA Recall Terminated Historical recordClass II

DICOPANOL (diphenhydramine hydrochloride in 5 mg/mL oral suspension kit) FusePaq, 150 mL Kits, Rx Only. Fusion Pharmaceuticals LLC., 768 Calle Plano, Camarillo, CA 93012. NDC: 43093-104-01.

by Fusion Pharmaceuticals, LLC

Reason
Microbial Contamination of a Non-Sterile Product: Kit component is contaminated with Burkholderia multivorans.
Published
March 18, 2015
Distribution
California

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FDA Recall Terminated Historical recordClass II

Dicopanol FusePaq Kit for Oral Suspension, 5mg/ML

by Fusion Pharmaceuticals, LLC

Reason
Microbial Contamination of Non-Sterile Products: Fusion Pharmaceuticals is recalling the Dicopanol FusePaq Kit due to Total Yeasts and Molds Count above USP limits.
Published
February 12, 2014
Distribution
CA

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Showing 1–2 of 2 results

This page lists recalls that name Fusion Pharmaceuticals, LLC as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.