Lifepak 500 Automatic External Defibrillator (2020-05-05)
Lifepak 500 Automatic External Defibrillator Recall Lifepak 500 Automatic External Defibrillators are being recalled across Canada due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk. The affected devices were distributed nationwide in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-05-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/688aae66-6d1b-4b09-a3b0-8833a17c8fe2