Zoom Latitude Programmer/recorder/monitor (2019-08-21)
Zoom Latitude Programmer/Recorder/Monitor Recall Zoom Latitude devices used to monitor and program heart implants are being recalled across Canada due to a medical device safety issue. The device can fail to properly communicate with implanted cardiac devices, potentially preventing necessary monitoring and programming functions. This recall affects all Zoom Latitude devices distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-08-30
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6aa40760-8e93-4b4d-8702-831d546b161a