Device Recall Digital Diagnost 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Philips Medical Systems North America Co. Phillips 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    44910
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0908-2007
  • 사례 시작날짜
    2007-07-23
  • 사례 출판 날짜
    2007-09-25
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-09-17
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    X-Ray System - Product Code MQB
  • 원인
    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.
  • 조치
    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.

Device

  • 모델명 / 제조번호(시리얼번호)
    Site numbers 103982, 104073, 105158, 105629, 504343, 505773.  Added sites: 104303, 38280, 44807, 59667, 76907, 76909, 76974, 82641, 82652, 82657, 82724, 83072, 83073, 84712, 84862, 84863, 86072, 86987, 86988, 102030, 102100, 102489, 102713, 102717, 102719, 102787, 102905, 102911, 103109, 103165, 103274, 103437, 103438, 103439, 103453, 103893, 103894, 103941, 104465, 104902, 104903, 104904, 104937, 104938, 105415, 105621, 105623, 105625, 105668, 250094, 250470, 250471, 250875, 500002, 504546, 504989, 505038, 505347, 505350, 505351, 505352, 505605, 505684, 505944, 506184, 506343, 506643, 506645, 506826, 506839, 506848, 519148, 519149, 519150, 519568, 519739, 519904, 520297, 520298, 520299, 520385, 520687, 520698, 520766, 520808, 520811, 520828, 520836, 520978, 520984, 520986, 521004, 521089, 521110, 521412, 521539, 521660, 521668, 521893, 521894, 521995, 521997, 522213, 522215, 522244, 522281, 522360, 522361, 522362, 522364, 522367, 522398, 522475, 530411, 530412, 530415, 530455, 530516, 530611, 530696, 530716, 530779, 530787, 530789, 530791, 530792, 530796, 530800, 530806, 531773, 531825, 531833, 531858, 531975, 531994, 531995, 532138, 532141, 532167, 532168, 532169, 532171, 532206, 532211, 532278, 532364, 532421, 532422, 532815, 532816, 532817, 532818, 533244, 533317, 533319, 533338, 533426, 533468, 533534, 533571, 533769, 533915, 533916, 533920, 533949, 533950, 534082, 534279, 534435, 534539, 534570, 534622, 534718, 534800, 534801, 534836, 534866, 535146, 535334, 535381, 535383, 535549, 535626, 535773, 535774, 535786, 535933, 536002, 536039, 536043, 536062, 536064, 536128, 536129, 536441, 536448, 536614, 536913, 536939, 537163, 537184, 537455, 537753, 537755, 537762, 537840, 537918, 537948, 537950, 537974, 538139, 538154, 538166, 538304, 538437, 538478, 539680, 540173, 540199, 540474, 540477, 542194, 543376, 545097, 549011, 549725, and 557777.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Units were distributed to 1543 hospitals and medical centers throughout the US. No international distribution from this firm.
  • 제품 설명
    Philips Digital Diagnost X-Ray system
  • Manufacturer

Manufacturer

  • 제조사 주소
    Philips Medical Systems North America Co. Phillips, 22100 Bothell Everett Hwy, Bothell WA 98021-8431
  • Source
    USFDA