Fujifilm Duodenoscope (2015-12-29)

Fujifilm Duodenoscope Recall Summary Fujifilm duodenoscopes (medical devices used to examine the small intestine) are being recalled in Canada. The recall is classified as Class I, meaning there is a serious risk of adverse health effects. These devices were distributed across Canada.

Reason

Health products

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-03-17

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c679d067-cc0b-48b4-a02e-f60425af332f