CE INFUSOR Patient Control Module Watch (PCM), 0.5 mL 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Baxter Healthcare 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2015-09-16
  • 사례 출판 날짜
    2015-09-16
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: baxter ce infusor patient control module watch (pcm), 0.5 ml the medicines and healthcare products regulatory agency (mhra), united kingdom posted a medical device safety alert concerning ce infusor patient control module watch (pcm), 0.5 ml [product code 2c1079k; lot number 15a056 and 15b047], manufactured by baxter healthcare. the manufacturer is issuing a recall for the above affected lots of the infusor pcm, 0.5ml due to complaints for partially detached back-plates on the underside of the device. a partial detachment of the pcm back-plate may cause an incomplete shut-off of the pcm watch tubing resulting in continuous flow of medication from the pcm to the patient. the manufacturer has identified the root cause of this issue and corrective actions have been implemented. the affected lots were produced prior to implementation of the corrective actions. continuous flow of pain medication to the patient may result in sedation, respiratory depression, or respiratory failure resulting in the need for medical intervention. these conditions could lead to serious injury or death. according to the local supplier, the affected products are not distributed in hong kong. for details, please refer to the mhra website:https://www.Gov.Uk/government/publications/safety-information-from-manufacturers-field-safety-notices/field-safety-notices-7-to-11-september-2015 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 16 september 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Baxter CE INFUSOR Patient Control Module Watch (PCM), 0.5 mL
  • Manufacturer

Manufacturer