Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device did not pass electrical safety testing for...
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 CardioTek BV directly.
Affected Products
CardioTek EP-TRACER Software V2.x.
Quantity: 146 units
Why Was This Recalled?
Device did not pass electrical safety testing for adequate insulation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CardioTek BV
CardioTek BV has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report