FDAJanuary 17, 2017device

Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliary tract via the upper GI tract. This anatomy includes, but is not restricted to, the organs; tissues; and subsystems: esophagus, stomach, duodenum, com...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Pentax initiated a field correction/safety alert for two (2) models of the Video Duodenoscope to determine how soiling may have occurred on the surface of the suction cylinder and under the distal cap during testing.

What to do

FDA enforcement status: Terminated

Brands named

pentax

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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