ClearanceBrief
Recall Z-0706-2025 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile

GE OEC Medical Systems, Inc

OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedures.

DateDec 18, 2024 (initiated Nov 21, 2024)
StatusOpen, Classified
ReasonDue to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
Root causeProcess control
ActionOn 11/21/2024, the firm sent an "URGENT MEDICAL DEVICE CORRECTION" Letter informing customers that GE HealthCare has become aware that recently manufactured OEC Elite and OEC 3D mobile C-arms, as well as recently replaced X-ray tubes on certain OEC Elite, OEC 3D and OEC 9900/OEC 9800 mobile C-arms potentially have insufficient sealing that can result in an oil leak. This issue could result in loss of fluoroscopic imaging capability. Customers are instructed to: 1.Continue to use their OEC Elite, OEC 3D, OEC 9900 and/or OEC9800 mobile C-arm. 2.If oil is found leaking from the X-ray tube on th
Quantity25 systems
DistributionU.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S.: Australia, Brazil, Canada, Chile, Costa Rica, India, Italy, Philippines, Poland, Portugal, Sweden,
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
K111551OEC(R) 9800, OEC(R) 9800 PLUS
Ge Oec Medical Systems, Inc., Oct 4, 2011
K132027OEC 9800 PLUS
Ge Oec Medical Systems, Inc., May 1, 2014