Dexamethasone Moxifloxacin
Presence of particulate matter - Glass like particles.
Every FDA drug recall initiated in 2025, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
778 recalls, newest first.
Presence of particulate matter - Glass like particles.
Lack of Assurance of Sterlity
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
Failed Impurities/Degradation Specifications
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Presence of particulate matter: potential presence of metal particulates in the product.
Presence of particulate matter: potential presence of metal particulates in the product.
Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
cGMP Deviations
cGMP Deviations
Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.
Subpotent product:out of specification assay results observed during long term stability testing.
Subpotent product:out of specification assay results observed during long term stability testing.
Subpotent product:out of specification assay results observed during long term stability testing.
Presence of Foreign Tablets/Capsules
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
Incorrect Product Formulation
Cross Contamination with Other Products