Lidocaine HCl in all strengths
Reason Lack of sterility assurance.
14,450 recalls · Class II, newest first
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Lack of sterility assurance.
Reason Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.
Reason Lack of Assurance of Sterility: Leakage of the peritoneal dialysis (PD) solution bag.
Reason Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
Reason Failed Stability Specifications:stability failure at 12 months, long term RT conditions.
Reason Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
Reason Presence of particulate matter
Reason Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
Reason Failed Stability Specifications
Reason GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Reason GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Reason GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Reason GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Reason GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Reason Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.