Llura Xper Fd10/10 - Main Unit, Allura Xper Fd10, Allura Xper Fd20 - Main Unit And Allura Xper Fd20/10 System - Main Unit (2018-07-17)
Recall Summary Philips is recalling Allura Xper FD10/10, Allura Xper FD10, Allura Xper FD20, and Allura Xper FD20/10 medical imaging systems distributed across Canada. The recall is classified as Class I, indicating a serious safety concern. These devices were distributed to healthcare facilities nationwide.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-08-02
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fbd8d304-870f-40b8-a3f0-797610ab3dc4