FDAApril 6, 2016device

Ureteroscope Intended to provide optical visualization of and therapeutic access to the Urinary Track. This anatomy includes but is not restricted to the organs, tissues and subsystems: Urethra, Bladder and Renal Pelvis. The instrument is introduced via the urethra when indications consistent wit...

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

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

pentax medicalpentax

Recall history

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

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