Genzyme Corporation recalls Lumizyme (alglucosidase alpha), 50 mg/vial, For Intravenous Infusion Only, Rx Only, Manufactured by Genzyme Corportatio…

Recall date

December 8, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0799-2016

FDA classification

Class III

Brand / firm

Genzyme Corporation

Sold / distributed

TN

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Lumizyme (alglucosidase alpha), 50 mg/vial, For Intravenous Infusion Only, Rx Only, Manufactured by Genzyme Corportation, Cambridge, MA 02142, NDC 58468-0160-1