Device Recall MIDAS TOUCH 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Olsen Medical 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
    36470
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0182-2007
  • 사례 시작날짜
    2006-08-29
  • 사례 출판 날짜
    2006-11-15
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2011-07-26
  • 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
    electrosurgical electrodes - Product Code JOS
  • 원인
    Testing conducted by the firm indicates that electrodes identified with certain part numbers may fall out from the electrosurgical pencil or handle presenting the potential for harm or injury to the patient and/or user.
  • 조치
    The firm issued an ''Urgent: Device Recall'' notification to their customers via letter and E-mail on 8/29/2006 and 8/30/2006. The letter informs the customers of this problem and asks that the customers contact their sub-accounts and notify them of the problem if they have further distributed any of the suspect part numbers. The letter also asks that the distributor/customer(s) have the subaccounts discontinue use of the product; and return the held product to the distributor (who in turn, should return the product to Olsen Medical for reimbursement). The customers are asked to complete and fax back to the recalling firm, an attached Acknowledgement form documenting receipt of the recall notification by the customer/employee with name and date received. The firm also asked that the customer supply information regarding the amount of inventory /shipped on a checklist. The amounts received are broken down on the Checklist by Lot Number with the amount of product in inventory and the amount of product shipped. These amounts are reported by the responders by ''pieces and cases'' on hand at the time that the notice was received.

Device

  • 모델명 / 제조번호(시리얼번호)
    4 inch Standard Electrodes - Model Number: 30-0002, Lot Numbers: 110201, 116228, 117331, 117985, 120959 and 000501; and 4 inch Modified Electrodes - Part Number: 30-0012, Lot Numbers: 110101, 113523, 113877, 114428, 114527, 115294, 115420, 119874, 120223, 120732 and 120883.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide, including USA, Japan, and New Zealand.
  • 제품 설명
    MIDAS TOUCH Electrosurgical/102 mm (4 inch) Blade Electrodes, Disposable, Sterile Single Use Device, Part #30-0012 and #30-0002. The electrodes are individually packaged in Tyvek bags with 12 packages per case.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Olsen Medical, 3001 W Kentucky St, Louisville KY 40211-1505
  • Source
    USFDA