Events

Device Recall Alphatec Souls Proximal/Distal Deployment Wrench 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Alphatec Spine, 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
    61756
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1676-2012
  • 사례 시작날짜
    2012-03-19
  • 사례 출판 날짜
    2012-05-29
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2012-06-20
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=108936
  • 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
    Intervertebral fusion device with bone graft, lumbar - Product Code MAX
  • 원인
    Alphatec spine has received several complaints (n+4) on the alphatec solus distal deployment wrench for twisting or bending, which has been discovered either during or after instrumentation use. a fifth complaint received in which it was reported that the spline tip of the alphatec solus proximal deployment wrench had sheared from the instrument upon use.
  • 조치
    Alphatec Spine sent an Urgent Medical Device Recall Notification dated March 30, 2012, to all affected customers. The notification letter informed customers of the removal/recall and included instructions on what to do with the recalled products. Initial letter was delivered via FedEx, and followed by telephone call with a total of 4 attempts. Customers were instructed to return all of the affected product. Upon receipt of of the Medical Device Recall Notification, customers were instructed to contact Alphatec Spine's Customer Service Department immediately for instructions on how to return the instruments and fill out the lower portion of this letter to confirm that they have read the notification and have taken all necessary removal actions: Customers should return a signed copy of the form to: Alphatec Spine, Inc. 5818 El Camino Real, Carlsbad, CA 92008 ATTN: Rand Jadan Forms may also be returned via email to rjadan@alphatecspine.com or fax to 760-431-0289. For questions regarding this recall call 760-431-9286.

Device

Device Recall Alphatec Souls Proximal/Distal Deployment Wrench
  • 모델명 / 제조번호(시리얼번호)
    Part Numbers: 25975 & 25976. Product Code(s): MAX. Market Clearance: 510(k) K102402.
  • 의료기기 분류등급
    Orthopedic Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Worldwide Distribution - USA (nationwide) and Germany
  • 제품 설명
    SOLUS Anterior Lumbar Interbody Fusion Spinal || Spacer System, Solus Proximal/Distal Deployment Wrenches, 510(k) K102402. || The Alphatec Solus Anterior Lumbar Interbody Fusion (AUF) System is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DOD) at one or two contiguous levels from L2-S1 with up to Grade 1 spondyiolisthesis or retrolisthesis at the involved level(s). DOD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should be skeletally mature and have had six months of non-operative treatment. The Alphatec Solus implant is intended to be used with autograft. The device is intended for use with supplemental fixation that is in addition to the integrated blades. The Alphatec Solus implant is intended for use with supplemental spinal fixation. Specifically, the Alphatec Solus implant is to be used with the Alphatec's Zodiac¿ Spinal Fixation System, Aspida" Anterior Lumbar Plating System, or the ILLlCO¿ MIS Posterior Fixation System. Intervertebral body fusion device.
  • Manufacturer
    Alphatec Spine, Inc.

Manufacturer

Alphatec Spine, Inc.
  • 제조사 주소
    Alphatec Spine, Inc., 5818 El Camino Real, Carlsbad CA 92008-8816
  • 제조사 모회사 (2017)
    Alphatec Holdings Inc.
  • Source
    USFDA