FDAApril 19, 2016device

Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a few millimeters to several centimeters.

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

The hazard

The latches of the frame adapter can be locked even if the locating pins of the frame adapter is not inserted into the corresponding holes in the coordinate frame.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

300006560023000073200130001527001300006550013000011800130000171002

Recall history

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

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