FDASeptember 11, 2020device

Synapse PACS Software Versions 5.1 and higher

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

The hazard

There is a potential for the wrong patient information may be displayed in the viewer or PowerJacket. Additionally, the incorrect max standard uptake values (SUV) for PET ad CT studies may be returned for Siemens Modality.

What to do

FDA enforcement status: Ongoing

Brands named

fujifilm medical systems ufujifilmfujifilm medical

Recall history

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

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