Events

Device Recall Philips brand BrightView Gamma Camera System, SYST, BRIGHTVIEWTILT, 3/8" 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Philips Medical Systems 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
    59077
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2872-2011
  • 사례 시작날짜
    2011-06-03
  • 사례 출판 날짜
    2011-07-22
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2012-11-06
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=101034
  • 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
    System, tomography, computed, emission - Product Code KPS
  • 원인
    The gap between the two parts of the table may permit pinches to occur on either patient's skin or other body parts; it has the potential for serious injury if a patient's finger is caught between the pallet and patient table resulting in broken finger bone.
  • 조치
    Philips Healthcare issued a Customer Information letter (Field Change Order (#88200402)) dated June 15, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to follow the instruction for use for their system, which states "Monitor the patient and the system vigilantly during any system motions to make sure that ...accessories, equipment, and all ojbects such as hair, jewelry, or neckties-remain clear of any moving camera and imaging table parts. For additional information, customers were istructed to see the BrightView SPECT instructions for Use, section 2.2 - Safety Warnings and Precautions and Safety and Information Labels. Philips Healthcare will notify all affected customers and will install a sticker through an Action for Performance - Proactive Field Change Order (FCO) to resolve the issue. For customers in North America who require further information or support contact Customer Care Solutions Center at 1-800-722-9377, Select Option 5. In all other countries the local Philips Healthcare office should be contacted.

Device

Device Recall Philips brand BrightView Gamma Camera System, SYST, BRIGHTVIEWTILT, 3/8"
  • 모델명 / 제조번호(시리얼번호)
    System Code: 882480;  Serial #s: 4000224, 4000061, 4000321, 4000043, 4000065, 4000081, 4000180, 4000044, 4000527, 4000298, 4000229, 4000262, 4000378, 4000280, 4000336, 4000324, 4000184, 4000190, 4000516, 4000303, 4000411, 4000305, 4000009, 4000012, 4000413, 4000213, 4000335, 4000436, 4000500, 4000491, 4000510, 4000518, 4000418, 4000454, 4000197, 4000353, 4000469, 4000005, 4000042, 4000379, 4000533, 4000451, 4000137, 4000343, 4000030, 4000540, 4000421, 4000342, 4000495, 4000511, 4000317, 4000338, 4000316, 4000408, 4000251, 4000031, 4000341, 4000122, 4000530, 4000395, 4000286, 4000294, 4000348, 4000296, 4000462, 4000463, 4000464, 4000419, 4000096, 4000476, 4340005, 4000484, 4000268, 4000382, 4000169, 4000447, 4000228, 4000442, 4000297, 4000047, 4000049, 4000488, 4000156, 4000412, 4000273, 4000337, 4000394, 4000194, 4000179, 4000401, 4000385, 4000504, 4000121, 4000109, 4000115, 4000257, 4000503, 4000105, 4000356, 4000333, 4000339, 4000107, 4000227, 4000233, 4000173, 4000400, 4000397, 4000398, 4000494, 4000256, 4000386, 4000168, 4000126, 4000154, 4000399, 4000272, 4000478, 4340004, 4000219, 4000243, 4000437, 4000376, 4000416, 4000485, 4000035, 4000515, 4000427, 4000142, 4000226, 4000519, 4000475 4000066, 4000183, 4000459, 4000461, 4000468, 4000210, 4000063 4000150, 4000217, 4000393, 4000420, 4000479, 4000300, 4000075, 4000080, 4000086, 4000013, 4000396, 4000481, 4000392, 4000157, 4000323, 4000374, 4000072, 4000237, 4000493, 4000354, 4000203, 4000167, 4000041, 4000407, 4000372, 4000133, 4000209, 4000299, 4000477, 4000314, 4000010, 4000539, 4000409, 4000134, 4000153, 4000373, 4000471, 4000163, 4000465, 4000082, 4000331, 4000282, 4000449, 4000216, 4000269, 4000415, 4000345, 4000208, 4000279, 4000254, 4000125, 4000201,
  • 의료기기 분류등급
    Radiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA (nationwide) and Puerto Rico and the countries of Australia, Austria, Bahrain, Belgium, Brazil, China, Chile, Columbia, Czech Republic, Denmark, Dominican Republic, Egypt, France, Greece, India, Iran, Israel, Italy, Japan, Lithuania, Malaysia, Mexico, Netherlands, Peru, Portugal, Russia, Saudi Arabia, Singapore, South Korea, Spain, Switxerland, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, and the United Kingdom.
  • 제품 설명
    Philips brand BrightView Gamma Camera System, || SYST, BRIGHTVIEW-TILT, 3/8", Model Number: 4535-602-79811; || Product is manufactured and distributed by || Philips Medical Systems (Cleveland), Inc., || Cleveland, OH || The BrightView Gamma Camera System is intended to produce images depicting the anatomical distributions of single photon emitting radioisotopes within the human body for interpretation by medical personnel.
  • Manufacturer
    Philips Medical Systems

Manufacturer

Philips Medical Systems
  • 제조사 주소
    Philips Medical Systems, 3860 N 1st St, San Jose CA 95134-1702
  • 제조사 모회사 (2017)
    Philips
  • Source
    USFDA