FDASeptember 22, 2020device

9310HD Digital Video Capture Module with software version 3.4.0 or higher configured with 9263 endoPortal

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

The hazard

There is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does not occur at the time the user performs and initially reviews an exam; it is not evident until a follow-up review occurs.

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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