Zurion 7 M12, M20 (2019-07-05)
Azurion 7 M12, M20 Recall Summary Philips is recalling Azurion 7 M12 and M20 imaging systems distributed across Canada due to a software issue that could affect device performance. The recall is classified as Class I, meaning there is a reasonable probability that use of the product will cause serious injury or death. This recall affects healthcare facilities that use these cardiac imaging systems.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-07-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/90405061-465d-42c2-b83a-1b450d67c9e5