Fore-sight Elite Tissue Oximeter Module

Fore-Sight Elite Tissue Oximeter Module Recall The Fore-Sight Elite Tissue Oximeter Module is being recalled in Canada because it may provide inaccurate measurement results. This device is used to monitor tissue oxygen levels. The recall is classified as Class I, meaning there is a serious potential health risk associated with the inaccuracy.

Product

Fore-Sight Elite Tissue Oximeter Module

Reason

Inaccurate test or measurement results

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2022-05-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/361c9b01-1474-4800-a4d0-66d5284a3ebb