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Alexion Pharmaceuticals, Inc.

No ongoing recalls currently shown

Based on the official records currently available to Public Health Trace, no recalls naming Alexion Pharmaceuticals, Inc. are currently shown as ongoing. The 2 records below are historical recall records.

Public Health Trace has 2 recalls naming Alexion Pharmaceuticals, Inc. as the recalling firm, republished from official FDA and USDA sources.

Recall history - 2 terminated records

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 TerminatedTerminated: May 29, 2015Historical 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 TerminatedTerminated: March 2, 2015Historical 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

View recall →

Showing 1–2 of 2 results

Some FDA recall records on this page come from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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.