Llura Xper Fd10 And Fd20 (2017-08-16)
Allura Xper FD10 and FD20 Recall Summary Philips is recalling Allura Xper FD10 and FD20 X-ray imaging systems distributed across Canada due to a software issue that could affect image quality and patient safety during cardiac procedures. The recall affects healthcare facilities that use these devices for diagnostic imaging. This is classified as a Class I recall, indicating a serious safety concern.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-09-11
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5200f7d2-70fe-45ed-bc2c-6dc9f3a1314e