Mobicath Bi-directional Guiding Sheath

Mobicath Bi-Directional Guiding Sheath Recall The Mobicath Bi-Directional Guiding Sheath, a medical device used in medical procedures, is being recalled across Canada. The recall is classified as Class I, which is the most serious type. This product was distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-10

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b78e0588-ed89-46a5-bf7d-16c8902b00fb