Lotrimin AF
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
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.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
cGMP Deviations
cGMP Deviations
cGMP Deviations
Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8
Failed Dissolution Specifications
Lack of Assurance of Sterility: Air filter failed post integrity test leading to a lack of sterility assurance.
Finished product specification did not meet USP specifications.
Lack of Assurance of Sterility
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Lack of Assurance of Sterility
Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.
CGMP Deviations: Use of this product may cause possible infection/ irritation of the skin and/or soft tissues.
Lack of sterility assurance.
Lack of sterility assurance.
Defective container: Cracked vials leading to lack of sterility assurance