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U.S. Department of Health and Human Services

Class 2 Device Recall Eclipse TPS

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 Class 2 Recall
Eclipse TPS
see related information
Date Posted September 23, 2008
Recall Status1 Open
Recall Number Z-1612-2008
Recall Event ID 46902
Premarket Notification
510(K) Number
K071873 
Product Classification System,Planning,Radiation Therapy Treatment - Product Code MUJ
Product Eclipse Treatment Planning System, Client 8.1.18 and DCF 8.1.17, model number H48
Code Information Serial numbers all starting with H48 (model number): 6509, 6974, 6616, 6688, 6806, 6568, 6530, 6839, 6740, 7178, 6700, 6694, 6505, 6924, 6979, 6715, 6556, 6757, 6820, 6545, 6564, 7027, 6783, 6553, 6760, 6904, 6907, 7037, 6639, 7088, 6702, 6659, 6940, 6802, 6856, 6944, 6841, 6870, 6874, 6928, 6913, 6614, 7009, 6951, 6493, 6758, 7030, 6453, 6704, 6555, 6691, 6914, 6739, 6846, 6685, 6473, 7015, 6875, 6566, 6599, 6818, 7020, 6799, 6804, 6699, 7075, 6901, 6827, 6833, 6681, 6724, 6499, 6698, 6722, 7018, 6782, 6893, 6522, 6937, 6708, 6560, 6977, 6978, 6803, 6961, 6503, 6814, 7029, 6707, 6686
Recalling Firm/
Manufacturer
Varian Medical Systems Oncology Systems
911 Hansen Way
Palo Alto, California 94304-1028
Manufacturer Reason
for Recall
A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan.
FDA Determined
Cause 2
DESIGN: Software Design
Action An Urgent Medical Device Correction letter was distributed October 2, 2007, to all direct consignees, informing them that the ARC treatment plans containing a Dose Dynamic MLC for IMRT delivery will not be recognized properly by the System. The firm provided corrective instructions and informed consignees that a product modification will be developed to resolve the issue. A Varian Service Representative will be scheduling a visit to upgrade the application.
Quantity in Commerce 90 units
Distribution Product was distributed throughout the USA (in LA, IN, GA, MD, IL, AR, CA, MA, FL, AZ, SC, MO, CO, AL, OK, WA, MI, IN, NY, TX, MS, NE, TN, VA, WI, OR, DC, and NC) and internationally (Japan, Columbia, Canada, India, Czech Republic, Turkey, Germany, Portugal, Venezuela, Australia, South Korea).
Total Product Life Cycle TPLC Device Report

 
1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database 510(K)s with Product Code = MUJ and Original Applicant = VARIAN MEDICAL SYSTEMS, INC.
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