Phenylephrine HCl
Reason Lack of Assurance of Sterility
11,815 recalls · Class II, newest first
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Reason Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Reason Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Reason Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Reason Sub Potent Drug: OOS results observed for the Hydrocortisone assay during routine stability testing at 12 month controlled room temperature.
Reason CGMP deviation: Trace amounts of impurity detected to be N-Methylnitrosobutyric acid (NMBA) in the API.
Reason Lack of Assurance of Sterility: preliminary environmental monitoring report exceeds limits, therefore sterility cannot be assured.
Reason CGMP deviation: Product found to contain trace amounts of NMBA
Reason Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two of the five items contained within the kit.
Reason CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified.
Reason CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen impurity, detected in the active ingredient.
Reason Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
Reason CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified
Reason CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified
Reason CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified
Reason CGMP Deviations:Traces amounts of N-Nitroso N-Methyl 4- amino butyric acid (NMBA) impurity found in Active Pharmaceutical Ingredient (API).
Reason Failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples.