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U.S. Department of Health and Human Services

Class 2 Device Recall GE Healthcare Innova 3100/ 3100 IQ

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  Class 2 Device Recall GE Healthcare Innova 3100/ 3100 IQ see related information
Date Initiated by Firm March 26, 2007
Date Posted July 10, 2007
Recall Status1 Terminated 3 on October 21, 2008
Recall Number Z-1044-2007
Recall Event ID 37733
510(K)Number K023178  K031637  K050489  K042053  K052412  K052157  
Product Classification Fluoroscopic Imaging System - Product Code MQB
Product GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular Imaging System)
Code Information 65049331 2035763100 3027443100 5033703100 6106483100 6619483100 7022333100 7028533100 8014793100 8157413100 9734293100 201996LAB1 207351YCL1 207662CL4 208227CATH2 214590PH3100 219326IN31 239513CRLAB1 239939CLA 251633PROV 281420LAB23100 303425CL4 305364P3100 316651INNOVA31 352333CATH1 352333CATH2 361857CATH1 361980INNOVA2 405272SCL2 406543IN3 413582C3100 414649CL3 414649CL4 415925INV1 423844CCL1 479441SP3100 480728LAB2 480821IN2 502587LAB1 508856IN2 512901NI3100 516562INNOVA8 516562INNOVA9 530244XC106 561548CL4 570476INNOVA31 573632CRC2 573882UMC1 610447CL1 610595CL1 610891CL1 616392INNOVA 617732IN9 618241GSI3100 708WESTSUB3100 717782INNOVA31A 718470INNOVA2 760242CATH1 775982CATH2 781340IN2 812450CATH1 812858GWLAB1 812858GWLAB2 814676C1 816478MC1 816943STJIC1 816985NKCI 847362CONCATH4 864255SFCL3 865481CCL2 870864LAB2 901516R3 903UT3100 904276CTH1 907562CATH1 909464IN3 909825VAINNOVA 913345MI1 916781INNOVA1 916781INNOVA1 918494IN31A 940626DCH3100 954987CCL9 970350CL1 970945CL1 405604D3100 405840OIC3100 412623LAB2 414647CL1 541MWHINNOVA 617789IN1 671GMHAINVA 770991CL1 41018VAS01 600098VA01 A5112597 A5125119 A5127281 A5162256 A5333035 B5274834 CS1006VA03 DPM32143 FI1064VA01 FPG86403 FPG93008 GE1005VA01 JO1000VA01 M4016034 M40480151 M4163030 M5480755 NO1005VA05 PL1082VA01 RU1142VA01 SA1010VA02 dpn88402 850060724 910064007 910162006 910163006 910163009 910163012 910163015 082416010006 082416020004 082416030003 082416040015 082416040018 082416040019 082416080001 082416100006 082416100013 082416110002 082416120007 082416120010 082416130015 082416130017 082416140002 082416150001 082416160003 082416160008 082416160009 082416190001 082416190003 082416190004 082416210003 082416210004 082416210006 082416210008 082416220008 082416220009 082416270002 082416300001 082416310003 082416310006 082449120007 0910064009X 834160003 910064008 920169007 YV0034 YV0042 YV0043 YV0044 YV0045 YV0046 YV0047
Recalling Firm/
Manufacturer		 General Electric Med Systems LLC
3000 N Grandview Blvd
Waukesha WI 53188-1615
Manufacturer Reason
for Recall		 Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.
FDA Determined
Cause 2		 Other
Action A "GE Healthcare Urgent: Safety Notice" dated January 24, 2007 was sent to consignees describing the product, problem, safety instructions, product correction and contact information.
Quantity in Commerce 168
Distribution Worldwide, including USA, Guam, Canada, Australia, China, India, Japan, Korea, Malaysia, New Zealand, Algeria, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, Italy, Jordan, Morocco, Norway, Poland, Russia, Saudi Arabia, Spain, Sweden, Switzerland, Syria, Turkey, and United Kingdom.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = MQB and Original Applicant = GE HEALTHCARE
510(K)s with Product Code = MQB and Original Applicant = GE MEDICAL SYSTEMS
510(K)s with Product Code = MQB and Original Applicant = GE MEDICAL SYSTEMS, INC.
510(K)s with Product Code = MQB and Original Applicant = GE MEDICAL SYSTEMS, LLC
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