FDASeptember 5, 2017drug

Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device. Manufactured by: Genentech, Inc. 1 DNA Way, South San Francisco, CA 84080-4990. NDC: 50242-0085-27

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

The hazard

Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.

What to do

FDA enforcement status: Terminated

Brands named

genentech

UPCs

50242008527

Recall history

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

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