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Covidien LLC recalls MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
Recalled September 9, 2015 · FDA recall Z-2545-2015 · Covidien
Hazard
Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns · FDA Class II
Units
7660 sets
Sold at
Nationwide Foreign: Canada Australia Denmark Germany New Zealand
Description
Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns
Product
MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC
Manufacturer(s)
Covidien LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →