3 FDA recalls mention Cetrorelix. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cetrorelix.
Reason Defective Delivery System: Missing or duplicated needles within the injection kit
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Reason Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
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