Llura Xper Fd10, Fd20, Fd10/10, And Fd20/10 (2018-06-12)
Recall Summary Allura Xper FD10, FD20, FD10/10, and FD20/10 medical devices distributed across Canada have been recalled. The recall is classified as Class I, which is the most serious type. No additional details about the specific reason for the recall or affected patients are provided in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-08-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a63215e3-113a-4806-a767-546a76958004