Oxoid Dryspot Legionella Pneumophila And Species Kit (2017-02-27)

Oxoid Dryspot Legionella Pneumophila and Species Kit Recall The Oxoid Dryspot Legionella Pneumophila and Species Kit, a medical device used to test for Legionella bacteria, has been recalled across Canada. The recall was issued due to a problem with the device itself. This affects laboratories and healthcare facilities that use this kit for testing.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-05-02

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/699428bb-d134-4106-a463-3c2aae7f11fe