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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device

Covidien LLC: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs Defibrillators; Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

Agency Publication Date: October 15, 2014
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Affected Products

Product: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R

All lots

Product: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Number: 22660PC

Al lot codes

Lot Numbers:
codes
Product: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660

Al lot codes

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Product: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006

Al lot codes

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codes
Product: MediChoice¿ Multifunction Electrode Part Number: MC171 OH

Al lot codes

Lot Numbers:
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Product: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A

Al lot codes

Lot Numbers:
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 69257
Status: Resolved
Manufacturer: Covidien LLC
Manufactured In: United States
Units Affected: 6 products (317,550 pairs; 9,850 pairs; 31,590 pairs; 133,930 pairs; 330 pairs; 151,210 pairs)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.