Philips Heartstart Onsite And Home Defibrillator And Heartstart Frx Automated External Defibrillator (2018-02-23)
Recall Summary Philips is recalling certain HeartStart OnSite, Home, and FRx defibrillators distributed in Canada due to a medical device issue. The specific defect or risk associated with these devices is not detailed in the provided information. This recall affects defibrillators that were distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-03-13
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/898ac790-122b-438f-857c-3d45002a6ecb