GE Healthcare Innova 4100 IQ Digital Fluoroscopic Imaging System (Vascular Angiography 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.
This recall has been terminated (originally issued September 30, 2008).
- Company
- Datex Ohmeda, Inc
- Recall Initiated
- August 17, 2006
- Posted
- September 30, 2008
- Terminated
- June 9, 2009
- Recall Number
- Z-1520-2008
- Quantity
- 71
- Firm Location
- Madison, WI
- Official Source
- View on FDA website ↗
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.
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
Lot / Code Info
serial number: 00000007C20046, 00000088514VE5, 00000453906BU0, 00000453949BU0, 00000464077BU7, 00000464473BU8, 00000477785BU0, 00000477790BU0, 00000477801BU5, 00000477819BU7, 00000477822BU1, 00000477831BU2, 00000477835BU3, 00000477837BU9, 00000477841BU1, 00000479528BU2, 00000489698BU1, 00000489699BU9, 00000489768BU2, 00000496743BU6, 00000497530BU6, 00000498660BU0, 00000499684BU9, 00000499708BU6, 00000505091BU9, 00000509178BU0, 00000509203BU6, 00000509244BU0, 00000509248BU1, 00000509254BU9, 00000511620BU7, 00000511652BU0, 00000511702BU3, 00000512694BU1, 00000512706BU3, 00000512710BU5, 00000512721BU2, 00000512824BU4, 00000512830BU1, 00000512832BU7, 00000512833BU5, 00000512863BU2, 00000512865BU7, 00000512881BU4, 00000512886BU3, 00000512893BU9, 00000512896BU2, 00000512908BU5, 00000513090BU1, 00000513142BU0, 00000513174BU3, 00000513198BU2, 00000513200BU6, 00000513203BU0, 00000513218BU8, 00000513227BU9, 00000513242BU8, 00000513243BU6, 00000513540BU5, 00000513550BU4, 00000513559BU5, 00000519098BU8, 00000526307BU4, 00000526310BU8, 00000526349BU6, 00000526385BU0, 00000526537BU6, 00000526676BU2, 00000526678BU8, 00000528507BU7, 00000528634BU9, 00000529470BU7, 00000529682BU7, 00000530250BU0, 00000544202BU5, 00000545958BU1, 00002UA63008FC, 000782415-0004. systems id: 574294IN41.
Root Cause
Radiation Control for Health and Safety Act
Action Taken
GE Field Engineers are visiting all affected customers to apply updated software. For assistance contact Datax-Ohmeda, Inc., at 1-608-221-1551.