Device Recall Orthos CM Bracket, Orthodontic Metal Bracket, 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Ormco Corporation 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
    61221
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-1136-2012
  • 사례 시작날짜
    2009-02-13
  • 사례 출판 날짜
    2012-03-01
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-03-02
  • 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
    Bracket, metal, orthodontic - Product Code EJF
  • 원인
    The recall was initiated because ormco has confirmed that manufacturing error resulted in the orthos cm brackets being incorrectly manufactured with a torque of -9¿. the packaging was labeled with +9¿ torque; however the brackets contained inside the packaging are actually orthos cm brackets with a torque of -9¿.
  • 조치
    Ormco Corporation sent an Urgent Field Safety Notice dated February 13, 2009, to all affected customers. The recall communication for consignees in the United States, Canada, Colombia, HongKong, Kuwait, United Arab Emirates, Mexico, Russia, South Africa and Croatia was sent on February 13, 2009 via USPS First Class Mail. The recall communication for consignees in Japan was sent on February 17, 2009. European consignees were sent recall notification on February 23, 2009. The Australian consignees and New Zealand consignees were the sent recall communication on February 25, 2009. Customers were instructed to contact Ormco Customer Care at (800) 854-1741 to receive an RMA number. The affected product should be returned to Ormco Corporation at the following address: Ormco Corporation, 1332 South Lone Hill Avenue, Glendora, CA 91740. Customers were instructed to label their return product "RECALLED PRODUCT Attention: Customer Returns". Customers were instructed to complete the enclosed Return Form and return it by fax to (909) 962-5605. For questions regarding this recall call 909-962-5600.

Device

  • 모델명 / 제조번호(시리얼번호)
    Part Number: Lot Number: 454-1210 08H599H 454-0210 08H358H, 08J174J, and 08J175J
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA (nationwide) and worldwide to Canada, Colombia, Hong Kong, Kuwait, United Arab Emirates, Mexico, Russia, South Africa, Croatia, Japan, France, Bulgaria, Germany, Estonia, United Kingdom, Hungary, Ireland, Italy, Netherlands, Australia, and New Zealand.
  • 제품 설명
    Brand name: Orthos CM Bracket, Orthodontic Metal Bracket, || Part Numbers: 454-1210, 454-0210. || The intended use of this device is a fixed attachment on a tooth which holds an archwire during orthodontic treatment.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Ormco Corporation, 1332 S Lone Hill Ave, Glendora CA 91740
  • 제조사 모회사 (2017)
  • Source
    USFDA