7 FDA recalls mention Cidofovir. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Cidofovir.
Reason Lack of Assurance of Sterility: complaints received about dried powder on the outside of bottle
Reason CGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.
Reason Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
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…
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…
Reason Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility…
Reason Presence of Particulate Matter: Particulate matter was found in some vials of Vistide (cidofovir injection).
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.