Bupivacaine HCl Injection
Reason cGMP deviations: Temperature abuse
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Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason cGMP deviations: Temperature abuse
Reason Labeling: Missing label on the vial
Reason Subpotent Drug: Out of specification for assay.
Reason CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Reason CGMP deviations: tablets cracking
Reason Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
Reason CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Reason CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
Reason Subpotent Drug: Out of Specification results for Assay
Reason CGMP Deviations: FDA analysis found product to contain acetaldehyde above specification limits.