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U.S. Department of Health and Human Services

Class 2 Device Recall GE Innova fluoroscopic imaging system with bolus chasing

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  Class 2 Device Recall GE Innova fluoroscopic imaging system with bolus chasing see related information
Date Initiated by Firm October 21, 2007
Date Posted September 29, 2008
Recall Status1 Terminated 3 on December 17, 2011
Recall Number Z-1516-2008
Recall Event ID 45538
510(K)Number K042053  
Product Classification fluoroscopic imaging system - Product Code MQB
Product GE Healthcare Innova 3100 Digital Fluoroscopic Imaging System with Bolus Chasing option.
Code Information 8613100, 77573841, 0910064009, 3018774100, 4103323100, 4103374100, 4103623100, 4105434100, 4438494100, 5138534100, 5703214100, 7083333100, 7278253100, 8019643100, 8595724100, 9408984100, 082416040017, 082416070004, 082416120006, 082416130013, 082416140003, 201541LAB2, 229228INNOV41V, 239436CATH1, 251435ICV5, 270688INN, 304255INNOVA, 304347INNOVA, 309691P3100, 310423INNOVA1, 313593IC1, 313593IC2, 314525SACL2, 315448RM4, 315448RM5, 316268INNOVAA, 319338VA4100, 325670CATH, 334286BSP, 352333VASC, 352376SP, 352401CATH, 352401VASC, 378INV31, 407SPECIALS, 409899LAB3, 413447CATH, 414961INN4100, 416756INNOVA, 417269SCLD, 478633INOV, 502587LAB4, 508856OR41, 516562INNOVA4, 516663INNOVA2, 518525LAB1, 540953INNOVA, 561266IN31, 563421CATHLAB8, 573632CRA, 573761SMA, 573815BCR1, 574535IN41, 574647IN41, 6012884100SP1, 601553CL3, 602239LAB4, 602239LAB6, 603778ECL1, 606833INNOVA, 614293LIBERTY1, 614293LIBERTY2, 615338CV2, 615769SKYCV2, 619340VA8, 619482INNOVA1, 619541INNOVA31, 619552INNOVA1, 626359INNOVA, 702616INNOVA, 7028803100A, 706774CCL5, 713794LAB7, 713794LAB9, 715369INN4100, 717217INN31, 717763INNOVA41, 717763OR4100, 718283INNOVA3, 718518CVL1, 724656ANG, 724773C1, 727725SPEC1, 731422CV1, 732294INOV, 757398INNOVA, 757736INNOVA, 765453INNOVA1, 770991CL3, 773792CL3100, 773NORWG3100, 803329CL31, 803329CL41, 804594CATH, 808547QCV2A, 812238LIB1, 812279INNOVA1, 812283IN31, 812450EP1, 812482INNOVA, 813972INTV, 816276SP1, 817255NH4100, 817433HSW3100, 83INNOVA1188379, 845365V19, 850678IN3100, 865541CCL5, 865693CCL3, 901726SP2, 903CSM4100, 904202CATH3, 904276SP, 908522LAB1, 909788INNOVA1, 918307SHIN4, 918744JC4100, 928779INNOVA1, 936266CL1, 956389INN31, 956632INN4100, 956994INN1, 956994INN2, 972487ANGIO1, 973971LAB3, BPINNOVA2, BPINNOVA3R, BPINNOVA3R, ECXV1406C, FHORLCL1, HC1536XR04, RU1550VA01, RU2457VA01, SLIN4100, YV0022, and YV0036.
Recalling Firm/
Manufacturer		 GE Healthcare
3000 N Grandview Blvd
Waukesha WI 53188-1615
Manufacturer Reason
for Recall		 Incorrect dose data: GE Healthcare has found that after 6 days and 4 hours without performing a system reset or a system reboot (turning it off/on), the displayed dose data on these systems (Innova 3100 / Innova 4100 with Bolus option) may be underestimated by up to 50%. In order to avoid this issue, it is necessary to perform a system reset or reboot every day. GE Healthcare is working on a c
FDA Determined
Cause 2		 Nonconforming Material/Component
Action GE sent all customers with affected units a letter on 11/15/07 titled Urgent Medical Device Correction. In the US this was sent by a traceable means (either US Postal Service with receipt acknowledgement (registered mail) or equivalent courier service such as FEDEX overnight Delivery). The letter was sent to 3 titles within the affected accounts; Hospital Administrator, Manager of Radiology/Cardiology and Radiologist/ Cardiologist. A correction letter identified a short term recommendation to perform a system reset or reboot every day and stated that a software correction will be installed at their site at no cost.
Quantity in Commerce 146 total
Distribution Worldwide Distribution: USA, Argentina, Australia, Canada, China, Germany, Japan, Mexico and Russia.
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 MEDICAL SYSTEMS, INC.
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