ClearanceBrief
Recall Z-1921-2010 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Ge Healthcare, Llc

Innova 2100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally, rotational imaging procedures.

DateJun 29, 2010 (initiated Jun 3, 2010)
StatusTerminated
ReasonGE Healthcare has become aware of a potential loss of gantry and table motions affecting Innova 2100IQ, 3100, 3100IQ, 4100 and 4100IQ systems with InnovaIQ Table that may impact patient safety.
Root causeDevice Design
ActionConsignees were sent on 6/3/10 a GE Healthcare "Urgent Medical device Correction" letter dated May 12, 2010. The letter was addressed to Hospital Administrators/ Risk Mangers, Managers of Radiology/Cardiology and Radiologists/ Cardiologists. The letter included the Safety Issue, Affected Product details, Safety Instructions, Product Correction and Contact Information. Customers are to contact a service representative immediately if they notice any cable damage.
Quantity10
DistributionWorldwide Distribution -- USA, including states of AL, AZ, CA, CO, FL, GA, IL, IN, KY, MA, MI, MS, MO, MT, NE, NJ, NY, NC, OH, OR, PA, TN, TX, VT, WA, WV, and WI and countries of UNITED KINGDOM, SWEDEN, REPUBLIC OF KOREA, NORWAY, NEW ZEALAND, ITALY, ISRAEL, IRELAND, INDIA, HONG KONG, GERMANY, FRANCE
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K023178INNOVA 4100
Ge Medical Systems, Inc., Nov 26, 2002
K031637INNOVA 3100
GE Medical Systems, Aug 22, 2003
K033244DIGITAL FLUOROSCOPIC IMAGING SYSTEM, MODEL INNOVA 4100 WITH TILT TABLE OPTION
Ge Medical Systems, Inc., Oct 16, 2003
K042053INNOVA 4100, INNOVA 3100
Ge Medical Systems, Inc., Aug 26, 2004
K050489INNOVA 2100
Ge Medical Systems, LLC, Mar 11, 2005