Pentax Duodenoscope & Medical Single Use, Sterile Distal End Cap With Elevator (2021-04-30)

Pentax Duodenoscope Recall Summary Pentax duodenoscopes and their sterile distal end caps with elevators are being recalled across Canada due to issues with the medical devices themselves. This recall is classified as Class I, meaning there is a serious potential health risk. The affected devices were distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-05-13

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ae804bce-be1f-4a1e-b31f-79cfb3bcf831