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-2368-2014
  • 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
    Accessories, operating-room, table (kit) - Product Code FWZ
  • 원인
    Customed has determined that there is the possibility that packaging integrity may be compromised on different 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 900-1042, 12 lots: 113026163 113036737 113046994 113057378 113078232 113078669 113089153 113109704 131110065 131110610 140111137 140312045
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 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
    ARTHROSCOPY PACK - || (1) SURGICAL DURAPREP SOLUTION 26ML LIF || (1) ESMARK BANDAGE || (1 ) ELASTIC BANDAGE 6" X 5yds LIF || (1) NEEDLE & BLADE COUNTER 20C FOAM/MAG || (1) TUBE SUCTION CONNECTING W X 12' LIF || (1) SHEET EXTREMITY ABS. 125" X 85" SMS || (1) DRAPE LASER CAMERA W/EL || (3) TOWELS ABSORBENT 15" X 20" LIF || (2) CONTAINER SPECIMEN 4oz. WITH LID & LABEL || (1) BABY BLANKET IMP. POLY ABS. LIF || (1) NEEDLE HYPODERMIC 20G X 1%'' || (10) GAUZE SPONGES 4" X 4" 16PLY || (1) BLADE SURGICAL #11 CARBON STEEL || (1) TABLE COVER REINFORCED 50" X 90" LIF || (1) IMPERVIOUS STOCKINETTE || (1) SHEET DRAPE 42" X 55" LIF || (1) SUTURE BAG FLORAL LIF || (1) U-DRAPE 60" X 70" WITH TAPE SPLIT || (1) MAYO STAND COVER REINFORCED LIF || (2) GOWN IMPERVIOUS REINFORCED SMS LARGE || (4) STRIPS TAPE || (1) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK LIF || (1) GAUZE KERLIX 4.5 X 4.1 YO 6PL Y || (1) GOWN IMPERVIOUS EXTRA REINFORCED X-LARGE TOWEL & WRAP || 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