Cardiolab System - Amplifier (2018-09-17)
CardioLab System - Amplifier Recall CardioLab System Amplifier units are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which is the most serious type. The affected devices were distributed nationwide in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-05-08
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/56a8c889-1415-48df-b2ca-4e2857fc8a93