FDAJanuary 10, 2024drug

Fosaprepitant for Injection 150 mg per vial, Sterile lyophilized powder for Intravenous use only after reconstitution and dilution, Single Dose Vial, Rx Only, Distributed by BE Pharmaceuticals Inc. 203 New Edition Court Cary, NC 27511, Made in India, NDC 71839-104-01.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Lack of Sterility Assurance: Aseptic process simulation failure.

What to do

FDA enforcement status: Terminated

Brands named

be pharmaceuticals ag

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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