FDA Enforcement Class II Terminated

Confocal GI Scope Intended to provide optical visualization of an therapeutic access to the Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum, and Large Bowel to the Cecum. The instrument is introduced via the mouth or rectum as decided by the anatomy being accessed when indications consistent with the need for procedure are observed in adult and pediatric patient populations.

Recall: Z-2069-2016 · Reported July 6, 2016

Enforcement

Recall Number
Z-2069-2016
Event ID
73894
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Pentax Medical Company
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 6, 2016
Initiation Date
April 6, 2016
Classification Date
June 28, 2016
Termination Date
December 21, 2017
Address
3 Paragon Dr, Montvale, NJ, 07645-1782, United States

Description

Confocal GI Scope Intended to provide optical visualization of an therapeutic access to the Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum, and Large Bowel to the Cecum. The instrument is introduced via the mouth or rectum as decided by the anatomy being accessed when indications consistent with the need for procedure are observed in adult and pediatric patient populations.

Reason

Pentax has become aware that operational/cleaning accessories and therapeutic devices (e.g., clips, stents, balloons, etc.) can become lodged in an endoscope's instrument channel.

Code Info

Model #'s EG-3870CIK, EC-3870CILK

Distribution

Worldwide Distribution - US (Nation Wide) including Puerto Rico and Internationally to Denmark, Guam

Quantity

17 units