[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
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
| Product | Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006 |
|---|---|
| Brand / manufacturer | Covidien LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0046-2015 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 18 September 2014 |
| EAN / barcode | 40000006 |
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.