Lidocaine HCl Injection
Lack of Assurance of Sterility
Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.
14,535 recalls, newest first.
Lack of Assurance of Sterility
Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.
Failed Impurities/Degradation Specifications - at 18-month Stability testing
Superpotent Drug
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
CGMP Deviations: sterile water not used for production
CGMP Deviations: sterile water not used for production
Lack of Assurance of Sterility
Failed Dissolution Specifications: below specification results
Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
CGMP Deviations
Defective container; yellow colored spike from cap lodged in the nozzle
Failed Dissolution Specifications
Subpotent Drug: reduced efficacy for epinephrine
CGMP Deviations: Out of Specification for Total Aerobic Microbial Count (TAMC) test for unfiltered bulk for decitabine for injection.
Failed Dissolution Specifications: results below specifications
Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.
Presence of particulate matter: glass
Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
CGMP Deviations: Out of specification for dissolution