Z-1519-2008

GE Healthcare Innova 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular imaging system). The Innova...

Name: Z-1519-2008 GE Healthcare Innova 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular imaging system). The Innova...
Creator: Datex - Ohmeda, Inc
Published: 2006-08-17
License: https://open.fda.gov/license/

GE Healthcare / initiated 2006-08-17 / Terminated

FDA source

Datex - Ohmeda, Inc began a recall of GE Healthcare Innova 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular imaging system). The Innova systems are indicated for use in generating... on 2006-08-17. The reason FDA records is "User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any preset exposure...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1519-2008
Status: Terminated
Initiated: 2006-08-17
Posted: 2008-09-30
Terminated: 2009-06-09
Recalling firm: GE Healthcare
Product: GE Healthcare Innova 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular imaging system). The Innova systems are indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally, rotational imaging procedures. They are also indicated for generating fluoroscopic images of human anatomy of cardiology, diagnostic, and interventional procedures. They are intended to replace fluoroscopic images obtained through image intensifier technology. These devices are not intended for mammography applications.
Product code: MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Reason for recall: User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any preset exposure time may lead to incorrect overall dose management, resulting in unnecessary exposure and can be a contributing factor for skin injury. The alarm can be heard in the control room.
FDA root cause: Radiation Control for Health and Safety Act
Action: GE Field Engineers are visiting all affected customers to apply updated software. For assistance contact Datax-Ohmeda, Inc., at 1-608-221-1551.
Quantity in commerce: 132
Distribution: within US: AL, AR, AZ, CA,CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and Puerto Rico. OUS to include: Algeria, Australia, Belgium, Brazil, Canada, China, Columbia, Denmark, Finland, France, Germany, Greece, Hungary, India, Indonesia, Ireland, Italy, Japan, Korea, Kuwait, Latvia, Malaysia, Mexico, New Zealand, Norway, Russia, Saudi Arabia, Singapore, Spain, Switzerland, Syria, Taiwan, Turkey, and United Kingdom
Product codes and lots: serial numbers: 00000007C20050, 00000061993GE2, 00000464046BU2, 00000464088BU4, 00000464127BU0, 00000477752BU0, 00000477766BU0, 00000477779BU3, 00000477793BU4, 00000477807BU2, 00000477808BU0, 00000477816BU3, 00000477827BU0, 00000477833BU8, 00000477840BU3, 00000479549BU8, 00000479577BU9, 00000485033BU5, 00000489690BU8, 00000489717BU9, 00000490496BU7, 00000491059BU2, 00000492423BU9, 00000493965BU8, 00000497494BU5, 00000498674BU1, 00000498692BU3, 00000498707BU9, 00000498882BU0, 00000498888BU7, 00000499681BU5, 00000499701BU1, 00000499702BU9, 00000499711BU0, 00000499720BU1, 00000499728BU4, 00000499936BU3, 00000505083BU6, 00000505109BU9, 00000509176BU4, 00000509205BU1, 00000509236BU6, 00000509237BU4, 00000509242BU4, 00000509243BU2, 00000509246BU5, 00000509252BU3, 00000509253BU1, 00000510040BU9, 00000511613BU2, 00000511672BU8, 00000511684BU3, 00000511685BU0, 00000511692BU6, 00000512738BU6, 00000512755BU5, 00000512825BU1, 00000512826BU9, 00000512829BU3, 00000512831BU9, 00000512834BU3, 00000512840BU0, 00000512866BU5, 00000512884BU8, 00000512889BU7, 00000512890BU5, 00000512897BU0, 00000512905BU1, 00000513093BU5, 00000513107BU3, 00000513112BU3, 00000513128BU9, 00000513172BU7, 00000513175BU0, 00000513183BU4, 00000513184BU2, 00000513189BU1, 00000513205BU5, 00000513267BU5, 00000513277BU4, 00000513278BU2, 00000513523BU1, 00000513527BU2, 00000513536BU3, 00000513544BU7, 00000513548BU8, 00000513549BU6, 00000513551BU2, 00000513570BU2, 00000513571BU0, 00000513576BU9, 00000513589BU2, 00000515118BU8, 00000518728BU1, 00000519107BU7, 00000519126BU7, 00000519153BU1, 00000520046BU4, 00000521647BU8, 00000526236BU5, 00000526308BU2, 00000526309BU0, 00000526348BU8, 00000526382BU7, 00000526383BU5, 00000526384BU3, 00000526386BU8, 00000526559BU0, 00000528646BU3, 00000529467BU3, 00000529510BU0, 00000529664BU5, 00000529681BU9, 00000530226BU0, 00000534470BU0, 00000534725BU7, 00000538734BU5, 00000538740BU2, 00000543268BU7, 00000545045BU7, 00000545590BU2, 00000546170BU2, 00000546434BU2, 00000546573BU7, 00000547027BU3, 00000547211BU3, 00000549174BU1, 00000772852-02, 00002UA6251HCZ, 00002UA6420FDN. systems id: 2667313, 82416040018, 82416130018.

Product code MQB

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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)