ClearanceBrief
Recall Z-2276-2023 ยท OWB Interventional Fluoroscopic X-Ray System

GE OEC Medical Systems, Inc

OEC 9800 Systems with 9-inch Image Intensifier

DateJul 31, 2023 (initiated May 15, 2023)
StatusOpen, Classified
ReasonImage intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.
Root causeProcess control
ActionOn 5/15/23 correction notices were mailed to: Director/Manager of Radiology, Hospital Administrator, Head of Radiology Department, PACS Administrator, Director of IT Department, Head, Biomedical Engineering, who were asked to do the following: You can continue to use your device. When transporting the device, ensure it is always in the Anterior Posterior (AP) position, as instructed in the systems Operator Manual. Use caution when moving system to avoid a large impact force. In addition, customers were asked to complete and return the acknowledgement response form to fieldactionssurgery@ge.c
Quantity58
DistributionWorldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY and the countries of Algeria, A
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