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[Recalled] Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006 — Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatibl… | FDA 2014-09-18

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductCovidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
Brand / manufacturerCovidien LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0046-2015
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date18 September 2014
EAN / barcode40000006

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Covidien LLC

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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