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Covidien LLC recalls Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Recalled October 22, 2014 · FDA recall Z-0046-2015 · Covidien
Hazard
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs · FDA Class I
Units
133,930 pairs
Sold at
Worldwide Distribtion-USA (nationwide) including Puerto Rico and the countries of Canada Greece Israel Belgium Finland France Germany Great Britain Ireland Italy Norway Poland Portugal Spain Sweden Switzerland Brazil Chile Philippines Taiwan Australia New Zealand.
Description
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
Product
Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Manufacturer(s)
Covidien LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →