Cetrorelix Acetate for Injection
Defective Delivery System: Missing or duplicated needles within the injection kit
Yes — there is an active recall. 2 ongoing FDA recalls mention Cetrorelix (3 total). Check the affected lots below.
Most common reason: Packaging defect (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cetrorelix. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Defective Delivery System: Missing or duplicated needles within the injection kit
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
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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