PHENYLephrine, 10mg/250ml added to 0.9% sodium chloride, 40mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc…
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
87 FDA recalls mention Phoenix. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Phoenix.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Reason CGMP Deviations
Reason Non-Sterility
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason Subpotent Drug: FDA analysis found product to be subpotent
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Reason CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
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