Iacs Monitoring Solution With C500 And C700 (2017-06-12)

Recall Summary The IACS Monitoring Solution with C500 and C700 devices are being recalled across Canada due to safety concerns classified as Class I (the most serious type). These medical monitoring devices were distributed throughout Canada and may pose a risk to users.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-07-07

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3c84d423-b602-4385-82d8-5104d6552d7c