FDAJanuary 2, 2015device

EPWorks software used in the Xltek Protektor Stimulator Product Usage: Intraoperative diagnosis of acute dysfunction in corticospinal axonal conduction brought about by mechanical trauma (traction, shearing, laceration, or compression) or vascular insufficiency.

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

The hazard

Software error occurs when using remote monitoring; if the remote user tries to stop the free run waveform group, the system will display a message informing the user that they do not have sufficient privilege.

What to do

FDA enforcement status: Terminated

Brands named

natus medicalnatus

Recall history

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

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