Device Recall Cannulated Drill Bits 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Synthes, Inc. 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
    71277
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1711-2015
  • 사례 시작날짜
    2015-05-13
  • 사례 출판 날짜
    2015-06-04
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2016-08-18
  • 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
    Bit, drill - Product Code HTW
  • 원인
    Affected parts and lots of the cannulated drill bits have the potential to break during use.
  • 조치
    DePuy Synthes sent an Urgent Notice Medical Device Recall letter dated May 13, 2015, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed if they have any of the identified devices, please take the following steps: " Call DePuy Synthes at 1-800-479-6329 to obtain a Return Authorization (RA) Number. " Complete the Verification Section (page 3 of this letter) by checking the appropriate box indicating affected product has been located. Also, please indicate the number of devices found and note the Return Authorization Number. Please include your name, title, address, telephone number and signature in the spaces provided. " Return the Verification Section (page 3 of this letter) with the product to: " Credit/Returns, DePuy Synthes, 1101 Synthes Avenue, Monument, CO 80132. " Send a copy of the completed Verification Section to DePuy Synthes by: " Fax: (888) 943-4893 or " Scan/email: Synthes6230@stericycle.com If you DO NOT have the identified product, please take the following steps: " Complete the attached Verification Section (page 3 of this letter) by checking the appropriate box indicating that no affected product has been located. Please include your name, title, address, telephone number and signature in the spaces provided. This return documentation acknowledges your receipt of medical device removal information. " Return the documents to DePuy Synthes by: " Fax: (888) 943-4893 or " Scan/email: Synthes6230@stericycle.com " Note: If the Verification Section is answered on behalf of more th An urgent medical device recall notice, dated May 13, 2015, was sent to consignees and sales consultants to in form them of the issue and associated risks. All in receipt of the device were asked to discontinue use and return affected devices along with the response form. Customers with questions were instructed to call 610-719-5450 or contact their DePuy Synthes Sales

Device

  • 모델명 / 제조번호(시리얼번호)
    Part Number  310.65 310.67 310.221  lot numbers  PE00966  PE01000 PE01039 PE01058 PE00959  PE00968 PE00974 PE00998 PE01006 PE01011 PE01048 PE00971  PE01059 PE01040
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - US (nationwide) and Canada.
  • 제품 설명
    3.2 mm Cannulated Drill Bit/ QC 170 mm || 2.7 Cannulated Drill Bit/ QC 160 mm || 2.0 mm Cannulated Drill Bit / QC 150 mm || there is no indication for Synthes Cannulated Drill Bits which is used with the Synthes Cannulated Screw. The Synthes Cannulated Screw, used with the threaded washer, is generally intended for intra-articular fixation of small bones, such as the hand, wrist, and forefoot.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Synthes, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
  • 제조사 모회사 (2017)
  • Source
    USFDA