Ventana He 600 Wash (2019-10-29)

Ventana HE 600 Wash Recall Summary Ventana HE 600 Wash, a medical device used in laboratory settings, is being recalled across Canada due to safety or performance concerns. This is a Class I recall, which indicates a serious issue. The recall affects all Ventana HE 600 Wash units distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-11-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9ae1787c-1cf6-41ba-90c8-5c41b33b64da