Liaison Control Measles Igm (2018-08-10)

LIAISON Control Measles IgM Recall Summary The LIAISON Control Measles IgM medical device has been recalled across Canada due to a device issue. This product is used in laboratory testing for measles antibodies. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cc3b611b-2e5e-413a-b9ce-4b28a50cdc28