FDA recalls about 244,432 carbamide peroxide ear drops nationwide for subpotent ingredient

The FDA is recalling about 244,432 containers of 6.5% carbamide peroxide earwax-removal products distributed nationwide due to subpotent active ingredient, potentially yielding ineffective results. The recall, classified as Class II, covers multiple brands (including CVS Health, Clinere, QC Quality Choice, TopCare Health, Audiologist's Choice, Family Wellness, Good Neighbor Pharmacy, Leader, Foster & Thrive, Meijer, CAREone) and advises consumers not to use these lots until replacement or further guidance is issued.