Events

Device Recall MDEleva, UDEleva 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Philips Medical Systems Nederlands 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
    79783
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1603-2018
  • 사례 시작날짜
    2018-03-26
  • 사례 상황
    Open, Classified
  • 사례 국가
    United States
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=163428
  • 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, x-ray, stationary - Product Code KPR
  • 원인
    The fixation of the upper and lower tilt actuator, of the md-eleva system might break off and the table will start to rotate from 0 to + 90 i- 90 degree with high speed. this rotating movement cannot be stopped by the user.
  • 조치
    The firm, BU IGT Systems, sent an "URGENT- Field Safety Notice" letter dated 3/23/2018 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to stop using the system and call your Philips representative if the following situations occurs: -the table height or tilt movement is not working. - you notice a cracking or snapping sound during system operation. - you experience a blockade in the table height or tilt movement during system movements. -the system is having an unexpected collision or the system had an unexpected collision in the past 2 months. - you have used a CPR stand that obstructed the system, or - you notice any (other) unusual system behavior beyond the normal use of the system. The customers should also avoid collisions with the table and base stand of the system by ensuring that no obstacles are placed around the system. In addition, ensure that all staff with access to the affected systems are informed of the content of this Field Safety Notice. The firm stated: -All possibly affected products in the field will be corrected by means of a field change order free of charge. -A firm representative will replace affected material on the upper and lower tilt actuator in the affected systems. -You will be contacted by our local Philips representative to schedule this corrective action. -This action will start effective April 2018. If you need any further information or support concerning this issue, please contact your local Philips representative: Technical Support Line: 1-800-722- 9377, 8am to 8pm (EST) Monday thru Friday.

Device

Device Recall MDEleva, UDEleva
  • 모델명 / 제조번호(시리얼번호)
    System Serial #  32 177 259 239 264 258 52 67 111 257 94 142 121 191 143 260 265 74 207 101 182 174 124 263 4 172 254 151 246 64 183 76 152 188 261 242 102 34 147 241 134 178 245 176 175 38 162 107 220 65 194 69 247 13 215 78 112 29 139 98 79 158 61 33 106 35 50 16 80 205 161 11 204 37 12 189 9 232 15 228 155 47 171 213 209 218 96 90 212 217 181 163 140 114 115 108 71 141 14 36 48 224 25 105 57 216 138 24 28 211 160 192 43 44 157 154 41 219 8 68 129 75 221 7 10 63 146 45 26 125 193 210 1 60 3 132 81 22 23 208 5 131 135 88 226 6 156 49 91 92 93 201 250 251 72 95 148 39 31 2 30 51 100 255 252 256 109 196 164 170 227 173 83 159 53 137 54 116 118 119 167 168 169 97
  • 의료기기 분류등급
    Radiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution: US (Nationwide) and countries of: Algeria, Argentina, Australia, Austria, Belgium, Canada, China, Colombia, Czech Republic, Denmark, Egypt, Estonia, Farce Islands, Finland, France, Germany, Hong Kong, Indonesia, Ireland, Israel, Italy, Jersey, Jordan, Korea, Republic of, Latvia, Lebanon, Luxembourg, Malaysia, Martinique Mexico, Netherlands, New Zealand, Norway, Oman, Philippines, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Thailand, Turkey, United Arab Emirates, and United Kingdom.
  • 제품 설명
    MultiDim Eleva 708032 || As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
  • Manufacturer
    Philips Medical Systems Nederlands

Manufacturer

Philips Medical Systems Nederlands
  • 제조사 주소
    Philips Medical Systems Nederlands, Veenpluis 4-6, Best Netherlands
  • 제조사 모회사 (2017)
    Philips
  • Source
    USFDA