Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006 Recalled by Covidien LLC Due to Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
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 Covidien LLC directly.
Affected Products
Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Quantity: 133,930 pairs
Why Was This Recalled?
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LLC
Covidien LLC has 248 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report