Z-0896-06

GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version...

Name: Z-0896-06 GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version...
Creator: GE Healthcare
Published: 2006-03-06
License: https://open.fda.gov/license/

GE Healthcare / initiated 2006-03-06 / Terminated

FDA source

GE Healthcare began a recall of GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. Cardiovascular Imaging System on 2006-03-06. The reason FDA records is "Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0896-06
Status: Terminated
Initiated: 2006-03-06
Posted: 2006-05-24
Terminated: 2008-02-24
Recalling firm: GE Healthcare
Product: GE Medical Systems Innova 2000 and Innova 2000S, and Innova 2000 and Innova 2000S mobile version. Cardiovascular Imaging System.
Product code: MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Reason for recall: Incorrect screws were used for mounting the detector which may lead to a possible part falling onto a patient.
FDA root cause: Other
Action: GEHC 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.
Quantity in commerce: 856 (534 domestic and 322 OUS)
Distribution: Nationwide 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 of Korea, Lebanon, Lithuania, Martinique, Mexico, Morocco, Netherlands, Norway, New Zealand, Poland, Portugal, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Republic of China, Thailand, Tunisia, Turkey, United Kingdom, Venezuela
Product codes and lots: all serial numbers

Product code MQB

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)