ClearanceBrief
Recall Z-0896-06 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

GE Healthcare

GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. Cardiovascular Imaging System.

DateMay 24, 2006 (initiated Mar 6, 2006)
StatusTerminated
ReasonIncorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.
Root causeOther
ActionGEHC is issuing a validated field action 3/6/2006 to correct the issues. Existing screws/bolts will be replaced using correct torque with screws containing cotter pins. Loctite liquid glue will be applied. Service manuals have been updated with instructions for using correct screws and torque. The field action is being implemented via Field Modification Instruction (FMI) 12033.
Quantity856 (534 domestic and 322 OUS)
DistributionNationwide including Puerto Rico and OUS to include: Australia, Belgium, Brazil, Bulgaria, Byelarus, Canada, China, Columbia, Czech Republic, Denmark, Egypt, Finland, France, Georgia, Germany, Greece, Honduras, Hungary, Indonesia, Iraq, Ireland, Israel, India, Iran, Italy, Jordan, Japan, Republic o
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