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-2512-2014
  • 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
    Orthopedic tray - Product Code OJH
  • 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)
    Code 900-2918, 8 lots 113047023 113057703 113068037 113078429 113078733 113109799 140312147 140613795
  • 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
    TLIF PACK || SURGICAL CENTER, CODE 900-2918. || CONTENTS: || (2) SOLUTION SURGICAL DURAPREP 26ML UF || (6) Pr. GLOVE SURG. DERMA PRENE # 8 PF UF || (4) GOWN SOFT SMS STD XL SET IN SLEEVE UF || (4) TOWELS ABSORBEN 15" X 20" LIF || (1) TABLE COVER REINFORCED 50" X 90" LIF || (1) MAYO STAND COVER REINFORCED LIF || (4) DRAPE% 60" X 76" REINFORCED L/F || (1) DRAPE CHEST 100" X 142" X 72" LIF || (1) FLUORO COVER 30" X 30" WITH RUBBBAND LIF || (2) LITE GLOVE LIF || (2) TUBE SUCTION CONNECT. Y." X 12' UF || (12) TOWELS CLOTH HUCK BLUE LIF || (1) UTILITY BOWL QUART 32oz || (10) GAUZE SPONGE 4" X 4" 16PLY XRD UF || (5) LAP SPONGE PREWASH 18" X 18" XRD LIF || (1) CAUTERY PENCIL ROCKER SWITCH WITH HOLSTER LIF || (1) STERI STRIP DRAPE LARGE 17" X 23" LIF || (1) SKIN MARKER WITH RULER UF || (9) LABELS FOR SKIN MARKERS 1.25 X Y2 || (1) RULER || (1) NEEDLE & BLADE COUNTER 20C FOAM/MAG L/F || (2) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK LIF || (2) SYRINGE 10cc WITHOUT NEEDLE LUER LOCK LIF || (1) BULB SYRINGE 60cc LIF || (4) NEEDLE HYPODERMIC 18G X 1Y2 UF || (1) NEEDLE HYPODERMIC 22G X 1Y2 LIF || (2) SYRINGE 3cc WITHOUT NEEDLE LUER LOCK UF || (1) NEEDLE SPINAL 18G X 6" LONG LENGTH LIF || (1) BLADE SURGICAL # 10 CARBON STEEL || (1) BLADE SURGICAL # 15 CARBON STEEL || (1) TIME OUT BEACON NON WOVEN UF || (2) DRESSING TEGADERM 4" X 4% "UF || (2) MEDICINE CUP 2oz || (1) DRAPE IOBAN INCISE 2 ANTIMICROBIAL 23" X 23" LIF || 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