FDAMay 22, 2020device

Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface to the FUJIFILM Synapse PACS Software (Server)

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

The hazard

Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be displayed incorrectly on the 3D TOMO slider bar. In addition, the slice location of the image and/or the slice direction could be incorrect as well, and result in misdiagnosis

What to do

FDA enforcement status: Ongoing

Brands named

fujifilm medical systems ufujifilmfujifilm medical

UPCs

0100358350110101421950151010080093778010080087818010035835016010133300034010080082385010080078513010133300007010133300020010148700002010080087409

Recall history

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

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