Dexamethasone - Moxifloxacin PF Injection
Lack of assurance of sterility: 13 vials were discovered to have faulty crimps.
832 recalls, newest first
Lack of assurance of sterility: 13 vials were discovered to have faulty crimps.
Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrect position on the product label making it illegible.
cGMP deviations: Vials may not be sealed correctly affecting sterility.
Subpotent Drug: Low out-of-specification assay results for the epinephrine component.
Failed Impurities/Degradation Specification: OOS for the following - unknown degradant/impurity, 4-chorobenzophenone, and for total impurities.
CGMP Deviations
Failed dissolution specifications: out-of-specification test results observed during the buffer stage dissolution testing.
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
Failed pH Specifications: Out of Specification pH Test Results were found in Sodium Chloride Injection USP 0.9% 2ml vial.
Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.
Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.
Failed Dissolution Specifications
Failed Dissolution Specifications
Labelling: Missing label.
Failed Dissolution Specifications
Subpotent drug
Subpotent drug
Subpotent drug