FDAJanuary 8, 2020device

Luminos dRF Max, model no. 10762471 - Product Usage: Luminos dRF Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial, skeletal, thoracic and lung ...

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

The hazard

A software bug may lead to one image to be assigned to two different patients, which could potentially affect medical diagnosis.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

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

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