FDAApril 6, 2016device

Intubation Scope Intended to provide optical visualization of, therapeutic access to, and use to facilitate routine or difficult tracheal intubations of the Upper Airway. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Larynx and Trachea. The instrument is int...

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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Intubation Scope Intended to provide optical visualization of, therapeutic access to, and use to facilitate routine or difficult tracheal intubations of the Upper Airway. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Larynx and Trachea. The instrument is int... — Recall Details · AllClear