ClearanceBrief
Recall Z-0681-2007 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

GE OEC Medical Systems, Inc

OEC 9800 MD Motorized C-Arm System, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT.

DateSep 28, 2007 (initiated Mar 1, 2007)
StatusTerminated
ReasonDuring routine service, primary and/or secondary collimators may not have been properly reinstalled.
Root causeOther
ActionCustomers were notified by letter on 03/01/2007. They were told to continue using the machines and that an inspection would be scheduled immediately to verify that collimators had been correctly installed.
Quantity70 units
DistributionNationwide and Germany.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K021049OEC 9800 PLUS DIGITAL MOBILE IMAGING SYSTEM
Ge Oec Medical Systems, Apr 17, 2002
K022069OEC FLUOROTRAK 9800 PLUS
Ge Oec Medical Systems, Sep 17, 2002
K024012OEC 9800 E/CV+ DIGITAL MOBILE IMAGING SYSTEM
Ge Oec Medical Systems, Mar 20, 2003