4 FDA recalls mention Ketotifen. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Ketotifen.
Reason CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity…
Reason CGMP Deviations: products were stored outside the drug label specifications.
Reason CGMP Deviations
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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