FDA Recalls Nearly 250,000 Containers of Carbamide Peroxide Due to Subpotency
The U.S. Food and Drug Administration (FDA) has announced a recall of approximately 244,432 containers of 6.5% carbamide peroxide. This recall is due to the products being subpotent, with only about 10% of the active ingredient present compared to the expected 6-7%. Carbamide peroxide is commonly used to soften and loosen earwax. The recall affects multiple brands, including CVS Health, Clinere, QC Quality Choice, TopCare Health, Audiologist's Choice, Family Wellness, Good Neighbor Pharmacy, Leader, Foster & Thrive, Meijer, and CAREone. The products were distributed nationwide and are packaged in 0.5-ounce bottles. The FDA has classified this as a Class II recall, indicating that the use of these products may cause temporary or medically reversible adverse health consequences.