Class II · Moderate risk
Ganirelix Acetate Injection
Failed impurities/degradation specifications: out of specification results for Ganirelix acetate acrylic acid adduct impurity.
Is Ganirelix recalled?
Yes — there is an active recall. 1 ongoing FDA recall mention Ganirelix (3 total). Check the affected lots below.
Most common reason: Impurity / degradation (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Ganirelix. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Ganirelix recalls on record
none so far in 2026; 3 on record, newest first
Class II · Moderate risk
Fyremadel (ganirelix acetate)
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Class II · Moderate risk
Ganirelix Acetate Injection
Failed Impurities/Degradation Specifications
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