EMD Serono, Inc. recalls Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EM
Recalled July 15, 2020 · FDA recall D-1379-2020 · EMD Serono
Hazard
Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance. · FDA Class II
Units
30,756 vials
Sold at
Nationwide in the US
Description
Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
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
Manufacturer(s)
EMD Serono, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →