Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Debrox Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to CGMP Deviations: products were stored outside the drug...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
Debrox, Carbamide Peroxide, Earwax Removal Aid, 0.5 FL OZ (15 mL) bottle per box), MedTech Products Inc., NDC 63029-321-01.
Quantity: 131 boxes
Why Was This Recalled?
CGMP Deviations: products were stored outside the drug label specifications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report