2% Lidocaine HCl Injectable Solution
Lack of Assurance of Sterility
11,818 recalls · Class II, newest first
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Sub Potent Drug: OOS results observed for the Hydrocortisone assay during routine stability testing at 12 month controlled room temperature.
CGMP deviation: Trace amounts of impurity detected to be N-Methylnitrosobutyric acid (NMBA) in the API.
Lack of Assurance of Sterility: preliminary environmental monitoring report exceeds limits, therefore sterility cannot be assured.
CGMP deviation: Product found to contain trace amounts of NMBA
Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two of the five items contained within the kit.
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified.
CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen impurity, detected in the active ingredient.
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified