Rapidpoint 500 System (2018-10-02)

RAPIDPoint 500 System Recall Summary The RAPIDPoint 500 System, a medical device used for blood testing, is being recalled across Canada due to safety or effectiveness concerns. This recall applies to all RAPIDPoint 500 Systems currently in use in Canada. The recall is classified as Class I, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-11-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3f7d414e-678f-4bc9-b3b8-6492e8882c66