Id-fungal Antibody System - Histoplasma (2016-05-11)

Recall Summary The ID-FUNGAL ANTIBODY SYSTEM - HISTOPLASMA test kit is being recalled across Canada due to a medical device issue. This laboratory diagnostic tool is used to detect antibodies to histoplasma fungus in patient samples. The recall affects healthcare facilities and laboratories that use this testing system.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-05-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/91465e52-3a76-4914-a04c-b017491b6823