Lifepak 1000 Defibrillator
LifePak 1000 Defibrillator Recall Summary Physio-Control is recalling LifePak 1000 defibrillators across Canada because the devices may fail to deliver a shock when needed due to a software problem. This defect could prevent the defibrillator from working properly during a cardiac emergency. The recall affects all LifePak 1000 defibrillators distributed in Canada.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-01-24
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2d8e4965-fd96-4117-8b38-bf8a766216c4