FDAMay 21, 2020device

Elekta Unity, Philips Marlin Software versions: R5.3.30, R5.3.31, R6.0.5331, R5.7.0, R5.7.1, R6.1.571

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

The hazard

In TSM (Treatment Session Manager) Motion Monitoring workflows, under certain conditions there can be a mismatch between the contour data overlay with respect to the motion monitoring images of the monitored structure.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

05060191071321

Recall history

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

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