7 FDA recalls mention Aprepitant. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Aprepitant.
Reason Presence of particulate matter: potential presence of metal particulates in the product.
Reason Lack of Sterility Assurance: Aseptic process simulation failure.
Reason cGMP deviations: Temperature abuse
Reason Labeling Error: Label Error on Declared Strength: Carton label and product insert incorrectly states the quantity of the excipient edetate disodium…
Reason Lack of Assurance of Sterility
Reason Shortfill: Aprepitant capsules 40 mg is being recalled due to customer reports of missing capsule in the blister pack.
Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…
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