Duodenovideoscope (2017-11-01)

Duodenoscope Recall Summary Pentax Medical duodenoscopes (endoscopes used to examine the small intestine) distributed across Canada are being recalled due to safety concerns with the medical device. The specific models affected include the ED-3490TK and ED-3490FK. This recall applies to healthcare facilities and medical centers that received these devices.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-11-30
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a7ef5cbe-761c-4944-ae52-112dcd60c8b2