Cobas It Middleware (2016-08-18)

Cobas IT Middleware Recall Summary Cobas IT Middleware was recalled due to issues with the medical device software. The recall was classified as Class I, meaning there is a serious potential for adverse health effects. The product was distributed across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/644bcc4f-6ca3-4acf-8479-f9c68e936e9d