6 FDA recalls mention Deferoxamine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Deferoxamine.
Reason CGMP Deviations: Firm failed to control impurity for color change at the API stage.
Reason Lack of Sterility Assurance
Reason Lack of Sterility Assurance
Reason Lack of Sterility Assurance.
Reason Lack of Assurance of Sterility: Sterility of product is not assured.
Reason Lack of sterility assurance.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.