FDAJuly 3, 2019device

GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.

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

The hazard

One bolt on the V motor was not fully tightened which caused a drift of .13 degrees in alignment resulting in reduced dose output.

What to do

FDA enforcement status: Terminated

Brands named

xcision medical systemsxcisionxcision medical

UPCs

00850002615005

Recall history

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

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