FDAJuly 27, 2020device

Flexible Intubation Video Endoscope, Part: 11301BNX, with Instruction Manual: Z18444US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.

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

The hazard

Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible intubation endoscopes with total lumen lengths greater than 850mm. Incompletely sterilized endoscopes might introduce infectious agents into patient airways, resulting in infection.

What to do

FDA enforcement status: Ongoing

Brands named

karl storz endoscopykarlkarl storz

Recall history

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

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