FDAJune 29, 2020drug
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
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
What to do
FDA enforcement status: Terminated
Brands named
emd seronoemd
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASchiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.2024-01-26
- FDALugol s Iodine Solution 500ML, Part Number 624-712023-10-17
- FDAClomiPHENE CITRATE Tablets, USP, 50 mg, 10-count (2 foil sealed plastic trays of 5 tablets each) per carton, Rx only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD., Jerusalem, 91010, Israel; Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960; NDC 0093-0041-03, UPC 3 009...2015-09-10
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