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U.S. Department of Health and Human Services

Class 2 Device Recall Easy Diagnost Eleva

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 Class 2 Recall
Easy Diagnost Eleva
see related information
Date Posted September 25, 2007
Recall Status1 Open
Recall Number Z-0910-2007
Recall Event ID 44910
Premarket Notification
510(K) Numbers
K023441  K031535  K032046  K945278  K970640  K982795 
Product Classification System, X-Ray, Stationary - Product Code KPR
Product Philips Easy Diagnost Eleva
Code Information Site numbers 506647, 522015, 542061, 542308, 543275, 543426102549, 102551, 103130, 103515, 103522, 103523, 103666, 104078, 104614, 104812, 105482, 105589, 105678, 105775, 105777, 500003, 500032, 504642, 504643, 504803, 504804, 504879, 504941, 504962, 504966, 505062, 505063, 505104, 505255, 505349, 505539, 505540, 505606, 505806, 505871, 505926, 506117, 506199, 506205, 506208, 506210, 506231, 506233, 506248, 506249, 506250, 506251, 506275, 506276, 506277, 506278, 506281, 506305, 506554, 506828, 506844, 506845, 519117, 519121, 519122, 519128, 519152, 519773, 519879, 519900, 520182, 520183, 520209, 520300, 520301, 520516, 520707, 520798, 520806, 521135, 521153, 521606, 521654, 521658, 521869, 521942, 522015, 522193, 522271, 522399, 522401, 522443, 522470, 522480, 530573, 530607, 530795, 530797, 530798, 531769, 531832, 531857, 531860, 532069, 532107, 532137, 532139, 532157, 532170, 532174, 532177, 532360, 532397, 532398, 532426, 532471, 532477, 532479, 532766, 532779, 532842, 532971, 532978, 533234, 533240, 533243, 533313, 533389, 533396, 533451, 533470, 533490, 533491, 533528, 533558, 533562, 533565, 533566, 533574, 533766, 533770, 533771, 533867, 533898, 533914, 533918, 533968, 534207, 534419, 534434, 534596, 534599, 534600, 534615, 534644, 534647, 534675, 534677, 534694, 534782, 534803, 534805, 534815, 534822, 534824, 534850, 534867, 534945, 535021, 535233, 535255, 535365, 535378, 535382, 535436, 535437, 535500, 535613, 535757, 535765, 535771, 535785, 535908, 535995, 536011, 536051, 536081, 536082, 536179, 536200, 536394, 536458, 536522, 536636, 536637, 536687, 536765, 536840, 536914, 536933, 536938, 536941, 536973, 536984, 536985, 536994, 537013, 537087, 537091, 537179, 537186, 537492, 537518, 537571, 537654, 537689, 537761, 537796, 537803, 537863, 537945, 537946, 537967, 537970, 537971, 538237, 538328, 538351, 538407, 538451, 538458, 538462, 538477, 538480, 538519, 538759, 538812, 538866, 538891, 538901, 539040, 539095, 539101, 539103, 539237, 539291, 539310, 539339, 539411, 539419, 539488, 539501, 539519, 539527, 539557, 539590, 539683, 539785, 540022, 540163, 540187, 540361, 540380, 540445, 540457, 540459, 540624, 540788, 540810, 541011, 541054, 541063, 541075, 541078, 541083, 541093, 541348, 541402, 541494, 541535, 541614, 541694, 541721, 541803, 541838, 541850, 541872, 541884
Recalling Firm/
Manufacturer
Philips Medical Systems North America Co. Phillips
22100 Bothell Everett Hwy
Bothell, Washington 98021-8431
For Additional Information Contact Sarah Baxter
425-487-7665
Manufacturer Reason
for Recall
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
FDA Determined
Cause 2
DESIGN: Software Design
Action On 7/23/07 Philips mailed a letter dated July 9, 2007 titled Electronic Product Radiation Warning. The letter advises customers of the issue and asks that customers apply the enclosed cautionary label to the device. The letter also explains that there will be a system modification to be installed. On 8/20/07 the firm sent the same letter, along with a letter dated 8/20/07 to customers thought to have either scrapped their units and the customer had previously indicated they were no longer using the unit. The 8/20/07 letter requested the customer contact Philps if they are currently using the device.
Quantity in Commerce 289 units
Distribution Units were distributed to 1543 hospitals and medical centers throughout the US. No international distribution from this firm.
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 = KPR and Original Applicant = PHILIPS MEDICAL SYSTEMS
510(K)s with Product Code = KPR and Original Applicant = PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO.
510(K)s with Product Code = KPR and Original Applicant = PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
510(K)s with Product Code = KPR and Original Applicant = PHILIPS MEDICAL SYSTEMS, INC.
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