Cequa (cyclosporine ophthalmic solution)
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
18,003 recalls, newest first
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
Subpotent
Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance impurities/degradation during routine stability testing.
Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.
Marketed Without an Approved NDA/ANDA
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Presence of foreign substance: Presence of stainless steel particulates in tablets.
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Chemical contamination: presence of benzene
Chemical Contamination; FDA analysis found product to contain benzene
Chemical Contamination; FDA analysis found product to contain methanol
Incorrect/Undeclared Excipient: Product contains alcohol
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Presence of Particulate Matter: Product was found to contain silica and iron oxide
Out of specification results observed in dissolution during long term stability testing.
CGMP Deviations: Failure to properly investigate failed microbial testing.
CGMP Deviations: Failure to properly investigate failed microbial testing.
CGMP Deviations: Failure to properly investigate failed microbial testing.
Microbial Contamination of Non-Sterile Products
Microbial Contamination of Non-Sterile Products