Human Igm Kit For Use On Spaplus (2018-07-25)

Recall Summary A Human IgM kit used with SPAPLUS laboratory equipment is being recalled across Canada due to issues classified as a Class I medical device concern. The recall affects users of this diagnostic kit in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/63c20723-7aae-4e5c-9eb4-692fe48307fa