drugs Class II Updated 2014-05-07

AbbVie Inc recalls LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) S

Recalled Product

LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose Administration Kit with prefilled dual-chamber syringe, 11.25 mg for 3-month administration, Rx only, Manufactured for: AbbVie Inc., North Chicago, IL 60064; by: Takeda Pharmaceutical Company Limited, Osaka, Japan 540-8645; NDC 0074-3779-03, UPC 3 00743 77903 5.

Hazard / Issue

Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #:1013566, Exp 12/08/16
View official government recall

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