Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028) Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Mitek identified that on VAPR Tripolar 90 Degree...
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 DePuy Mitek, Inc., a Johnson & Johnson Co. directly.
Affected Products
VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)
Quantity: 127
Why Was This Recalled?
Mitek identified that on VAPR Tripolar 90 Degree Suction Electrode the ablation and coagulation buttons are colored incorrectly. The wiring for each button function was confirmed as correct and the non-conformance impacted button color only
Where Was This Sold?
This product was distributed to 11 states: AL, CA, CT, FL, KY, MN, MS, NJ, NM, ND, TX
About DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek, Inc., a Johnson & Johnson Co. has 51 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report