Pentax Video Duodenoscope (2018-07-20)

PENTAX Video Duodenoscope Recall Pentax video duodenoscopes (endoscopy devices used to examine the small intestine) are being recalled in Canada due to concerns related to the device itself. This recall affects duodenoscopes that were distributed across Canada. The FDA classified this as a Class I recall, indicating a serious issue with the medical device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d9a3352b-aa0e-486c-ae39-6197bdd3b05c