Pentax Video Duodenoscope

Pentax Video Duodenoscope Recall Summary Pentax video duodenoscopes are being recalled in Canada due to a defect that prevents proper cleaning and disinfection of the instrument's internal channels, which could allow bacteria to remain on the device and potentially contaminate patients during medical procedures. This recall affects all Pentax video duodenoscopes distributed across Canada. The recall is classified as Class I, indicating a serious safety risk.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-04-13

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cd2bd8fc-ddbb-4628-adc3-1a52f92f0a4d