Class II
Terminated
Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose Administration Kit with prefilled dual-chamber syringe, 22.5 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 0074-3346-03, UPC 3 00743 34603 9.
- Company
- Abbvie Inc.
- Recall Initiated
- March 10, 2014
- Posted
- May 7, 2014
- Recall Number
- D-1287-2014
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 7362 kits
- Firm Location
- North Chicago, IL, United States
Reason for Recall
Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.
Distribution
Nationwide and Puerto Rico
Lot / Code Info
Lot #: 1014204, Exp 10/11/15; 1014485, Exp 12/11/16; and 1015007, Exp 12/06/16
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