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Alexion Pharmaceuticals, Inc.

Recalls

Recalls by year

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

Recalls by year
YearRecalls
20142
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FDA Recall Terminated Historical recordClass I

Soliris (eculizumab), 300 mg/30 mL (10 mg/mL), 30 mL Single-Use Vial, Rx only, Manufactured by: Alexion Pharmaceuticals, Inc., Cheshire, CT 06410, NDC 25682-001-01, UPC 3 25682-001-01 6.

by Alexion Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter: Product failed the appearance for the presence of visible particles under labeled storage condition.
Published
August 13, 2014
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only, 300 mg/30 mL (10 mg/mL), 30 mL Single-Use Vial, Rx only, Manufactured by: Alexion Pharmaceuticals, Inc., Cheshire, CT 06410, NDC 25682-001-01, UPC 3 25682-001-01 6.

by Alexion Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter: Failed the appearance test for the presence of visible particles.
Published
February 5, 2014
Distribution
Nationwide

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Showing 1–2 of 2 results

This page lists recalls that name Alexion Pharmaceuticals, Inc. 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.