Drug recall D-1379-2020

Class II Terminated reported Jul 15, 2020

Product

Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD 02370, NDC: 44087-1225-1

Reason for recall

Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.

Lots and codes

Lot # 8J025A; 8J025B, Exp 09/30/2020

Recall details

Recalling firm
EMD Serono, Inc., Rockland, MA
Quantity
30,756 vials
Distribution
Nationwide in the US
Type
Voluntary: Firm initiated
Recall initiated
June 29, 2020
Terminated
March 11, 2022

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