Llura Xper Fd 10 And Fd 20 Systems (2016-02-18)
Recall Summary Allura Xper FD 10 and FD 20 Systems have been recalled across Canada due to a medical device issue. These are X-ray imaging systems used in medical facilities. The recall is classified as Class I, indicating a serious potential health risk.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-03-04
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/95fb25be-06e3-4b54-bd6b-5dd05307ae14