Class II · Moderate risk
Fosaprepitant for Injection 150 mg per vial
Lack of Sterility Assurance: Aseptic process simulation failure.
Is Fosaprepitant recalled?
Not under an active recall.
Fosaprepitant was recalled 3 times in the past — all now closed. Most recent: Jan 10, 2024.
Most common reason: Sterility / contamination (2 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Fosaprepitant. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Fosaprepitant recalls on record
none so far in 2026; 3 on record, newest first
Class III · Low risk
Fosaprepitant for Injection
Labeling Error: Label Error on Declared Strength: Carton label and product insert incorrectly states the quantity of the excipient edetate disodium (EDTA) as 5.4 mg / vial, rather than the actual amount of 18.8 mg / vial.
Class II · Moderate risk
FOSAPREPITANT 150 mg/150 ml NS IVPB
Lack of Assurance of Sterility
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