ClearanceBrief
Recall Z-2435-2008 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

GE Healthcare

Innova 2000; The principle system components include a C-arm, image acquisition, processing and archiving capabilities. Indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally, rotational imaging procedures. Also indicated for generating fluoroscopic images of human anatomy for cardiology, diagnostic,

DateSep 20, 2008 (initiated Jul 25, 2008)
StatusTerminated
ReasonThe charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
Root causeDevice Design
ActionConsignees (Hospital Administrators; Hospital Risk Management Department; Mangers of Radiology/Cardiology; Radiologists/Cardiologists) were sent a "GE Urgent Medical Device Correction" letter dated July 2008. The letter described the affected products; the problem; and the user instructions, which state that the hospital should establish emergency workflow procedures to ensure patient safety should a component stop operating during a patient examination. Facilities should verify if their system has been impacted by checking if the catalog numbers listed are referenced on the PDB panel located
Quantity591
DistributionNationwide Distribution --- including states of CA, FL, NY, AK, AL, AR, AZ, PA, FL ,CO, SC, CT, IA, DC, DE, GA, HI, IL , IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NJ, MS, MT, NC, ND, NE, NH, NJ, NM, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and GUAM.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K022322INNOVA AND INNOVA 2000 S
Ge Medical Systems, Inc., Oct 8, 2002
K024200INNOVA 2000 AND INNOVA 2000S (MOBILE VERSION)
Ge Medical Systems, Inc., Jan 16, 2003
K993037LCV+ VERSION 2
Ge Medical Systems, Inc., Feb 14, 2000