Lifepak15 Monitor/defibrillator (2020-01-01)
LifePak15 Monitor/Defibrillator Recall Philips is recalling LifePak15 monitor/defibrillator devices distributed across Canada due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk associated with the devices. This recall affects LifePak15 units that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-01-20
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/7627af24-5962-4a22-a5c3-6d38c07ddff0