Device Recall Customed 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Customed, 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
    68536
  • 사례 위험등급
    Class 1
  • 사례 연번
    Z-2428-2014
  • 사례 시작날짜
    2014-05-20
  • 사례 출판 날짜
    2014-08-29
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2017-08-14
  • 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
    General surgery tray (kit) - Product Code LRO
  • 원인
    Customed has determined that there is the possibility that packaging integrity may be compromised on differ catalog numbers (multiple lots). this could result in an injury to the patient due to product contamination or loss of sterility condition.
  • 조치
    Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540

Device

  • 모델명 / 제조번호(시리얼번호)
    Product code 900-2003, 29 lots: 112030702 112041277 112062472 112093923 112103923 112114386 112114472 112125311 113015438 113025954 113026205 113036457 113047011 113047156 113057447 113057696 113057814 113068159 113078779 113089205 113099569 131110221 131110405 131110582 140211725 140211874 140312378 140312461 140412832
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
  • 제품 설명
    GENERAL PACK - || CONTENTS: (4) ABSORBENT TOWEL 15" x 20" LIF || (1) MAYO STAND COVER REINFORCED LIF || ( 1) NEEDLE & BLADE COUNTER 20c FOAM/MAG LIF || (2) UTILITY BOWL 16 oz. LIF || (1) GLASINE BAG PLAIN || ( 1) SUTURE BAG FLORAL || (4) DRAPE UTILITY WITH TAPE LIF || ( 1) TABLE COVER REINFORCED 50" X 90" LIF || (1) SURGICAL BLADE# 10 STAINLESS STEEL || ( 1) SURGICAL DURAPREP SOLUTION 26mL LIF || ( 1) LAPAROTOMY T DRAPE STD SMS || (2) DRAPE SHEET 41" X 58" SMS LIF || (2) GOWN IMPERVIOUS REINFORCED X-LARGE SMS LIF || (1 0) GAUZE 4"X 4" X 4 PLY || ( 1) CAUTERY TIP POLISHER LIF || (5) LAP SPONGES PRE-WASH XRD LIF || ( 1) CAUTERY PENCIL ROCKER SWITCH LIF || (1 0) GAUZE SPONGE 4" X 4" 16 PLY XRD LIF || ( 1) TUBE SUCTION CONNECT. 3/16" X 12' LIF || ( 1) SURGICAL BLADE# 15 CARBON STEEL || ( 1) CONTAINER SPECIMEN 4 oz. WITH LID & LABEL || Product Usage: || EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents
  • Manufacturer

Manufacturer

  • 제조사 주소
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • 제조사 모회사 (2017)
  • Source
    USFDA