Human Igm Kit For Use On Spaplus (2018-10-23)

Recall Summary A Human IgM kit used with SPAPLUS testing equipment is being recalled across Canada because it is classified as a medical device with a Class I issue. The recall affects all Canadian locations that received this product.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-11-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6078910b-c871-479e-9dff-4a3594faa482