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U.S. Department of Health and Human Services

Class 2 Device Recall EPIQ 5 Ultrasound System iwth Pediatric Cardiology option

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  Class 2 Device Recall EPIQ 5 Ultrasound System iwth Pediatric Cardiology option see related information
Date Initiated by Firm April 10, 2015
Date Posted May 05, 2015
Recall Status1 Terminated 3 on February 29, 2016
Recall Number Z-1578-2015
Recall Event ID 71084
510(K)Number K132304  
Product Classification System, imaging, pulsed doppler, ultrasonic - Product Code IYN
Product EPIQ 5 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 5G, EPIC 5C, EPIQ 5W. Catalog Number: 795204 / 795205. Part Number: 989605408541 With
453561736761 (1.1)
453561750041 (1.1.1)
453561753651 (1.1.2)
453561772231 (1.2)
453561772611 (1.2.1)
453561786571 (1.2.2)
453561785081 (1.3)
453561800581 (1.3.1)
453561805181 (1.3.2)
Code Information *********************SYSTEM CODES IN THE US***********************************  US114C0108, US114C0206, US114C0210, US114C0239, US114C0240, US114C0241, US114C0271, US114C0272, US114C0273, US114C0286, US114C0321, US114C0322, US114C0331, US114C0332, US114C0333, US114C0334, US114C0444, US114C0534, US114C0605, US114C0674, US115C0140, US115C0382, US115C0468, US214C0106, US214C0143, US214C0144, US214C0192, US214C0534, US214C0535, US214C0536, US215C0071, US215C0394, US215C0536, US215C0774, US215C0839, US215C0843, US215C0844, US215C1010, US215C1049, US215C1050, US314C0055, US314C0073, US314C0235, US314C0296, US314C0297, US314C0322, US314C0444, US314C0446, US314C0557, US314C0613, US314C0746, US314C0835, US315C0055, US414C0014, US414C0035, US414C0069, US414C0158, US414C0376, US414C0377, US414C0616, US514C0044, US514C0045, US514C0046, US514C0084, US514C0085, US514C0149, US514C0175, US514C0338, US514C0373, US514C0374, US514C0375, US514C0473, US514C0474, US514C0639, US514C0657, 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USO14C0157, USO14C0158, USO14C0159, USO14C0160, and USO14C0188.   *****************************SYSTEM CODES IN CANADA********************  US115C0274, US115C0466, US115C0467, US115C0494, US214C0486, US215C0034, US215C0036, US215C0347, US414C0111, US414C0112, US414C0113, US414C0114, US414C0477, US414C0478, US514C0339, US614C0688, US614C0854, US914C0179, US914C0180, USN14C0237, and USO14C1093.   ****************************SYSTEM CODES IN OTHER COUNTRIES*************  US114C0077, US114C0078, US114C0079, US114C0080, US114C0105, US114C0106, US114C0109, US114C0190, US114C0191, US114C0284, US114C0285, US114C0361, US114C0362, US114C0365, US114C0378, US114C0405, US114C0406, US114C0407, US114C0443, US114C0505, US114C0531, US114C0533, US114C0672, US114C0673, US114C0675, US114C0730, US114C0751, US115C0018, US115C0055, US115C0097, US115C0098, US115C0099, US115C0215, US115C0275, US115C0383, US115C0449, US115C0450, US115C0463, US115C0564, US115C0566, US115C0573, US115C0574, US115C0616, US115C0647, 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USO13C0683, USO13C0685, USO14C0051, USO14C0052, USO14C0053, USO14C0096, USO14C0125, USO14C0185, USO14C0186, USO14C0187, USO14C0478, USO14C0601, USO14C0602, USO14C0603, USO14C0604, USO14C0605, USO14C0606, USO14C0721, USO14C0845, USO14C1091, USO14C1124, USO14C1125, USO14C1126, USO14C1127, and USO14C1180.
Recalling Firm/
Manufacturer
Philips Ultrasound, Inc.
22100 Bothell Everett Hwy
Bothell WA 98021-8431
For Additional Information Contact Philips Customer Service
800-722-9377
Manufacturer Reason
for Recall
When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set up to Metric and weight and/or height is entered, a unit conversion error may result in the incorrect calculation of the patients Body Surface Area (BSA).
FDA Determined
Cause 2
Software design
Action Philips sent the Urgent-Medical Device Correction-Philips Model EPIQ5 and Ultrasound system letter, dated 2015 APRIL 10, and the Urgent-Medical Device Correction-Philips Model EPIQ7 and Ultrasound system letter, dated 2015 APRIL 10, letters to their consignees. These systems WITH Pediatric Cardiology option are affected. Philips issued two Field Change Orders (FCO) to their Field Service Engineer to install upgraded software: -FCO 79500336 for EPIQ5 -FCO 79500337 for EPIQ7 Customers with questions can call Philips Customer Service at 1-800-722-9377.
Quantity in Commerce 751 units total (246 units in the US and 505 units outside the US)
Distribution Worldwide Distribution - US (nationwide and DC) and Internationally to Norway, India, New Zealand, Bahrain, Sweden, Italy, Australia, France, Netherlands, Switzerland, Germany, Austria, and Turkey.
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 = IYN and Original Applicant = PHILIPS ULTRASOUND, INC.
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