FDA Records Ongoing Class II Recall of LEADER Carbamide Peroxide 6.5% Ear Drops
An FDA enforcement report lists 5,471 units of the 0.5 fl oz product recalled nationwide as subpotent, with the action initiated June 25, 2026.
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An FDA enforcement report lists 5,471 units of the 0.5 fl oz product recalled nationwide as subpotent, with the action initiated June 25, 2026.
An ongoing nationwide recall of a single lot "Lot:1505141", "exp 2027-04." cites a sub-potent drug with low pH and a significantly reduced assay, according to the agency's enforcement record.
The agency's enforcement report cites a sub-potent drug with low pH and a significantly reduced assay; the recall is listed as ongoing.
An FDA enforcement report lists 11,977 units of a carbamide peroxide 6.5% kit recalled nationwide as subpotent, with the action still ongoing.
An FDA enforcement report lists 15,843 units of the 6.5% ear drops recalled by Bell Pharmaceuticals, Inc for reduced potency; the action is ongoing.