Allura Xper Fd10 And Fd20/10 (product Of Alluraclarity Family)

Recall Summary Allura Xper FD10 and FD20/10 medical devices are being recalled across Canada due to a software defect. This is a Class I recall, which indicates a serious issue. The devices are part of the Alluraclarity family of products used in medical settings.

Product

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)

Reason

Software defect

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-11-25

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/658787b5-fba5-4b83-bb99-998879ac1955