FDAFDA · Food and drugs·Recall number Z-0048-2015
Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
Published October 22, 2014 · Recall initiated: September 18, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not Compatible for use with Philips model FR3 or FRx AEDs
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Covidien LLC
- Distributor
- 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.
- Lot
- Al lot codes
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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