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-2455-2014
  • 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
    Ear, nose, and throat surgical tray (kit) - Product Code OGR
  • 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 900-2423 ,3 lots 131010019 140111210 140312131
  • 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
    EAR PACK || CONTENTS: || (I) CAUTERY PENC IL ROCKER SW I TI-I CH ( I ) EMESIS BASIN l Oin 700cc || (2) LABEL FOR SKIN MARKERS || ( I) NEEDLE HYPODERMIC 1 80 X I Y, || ( I) WASI-l BASIN ROUND 6QT || (I) INSTRUMENT POUCH 7 X I I 2 COMPART || (I) STRIP STER I CLOSURE W' X 4" LIF || (I) SYRINGE 3cc W/0 NEEDLE LILOCK L/F (2) SY RI NGE I ML W/0 NEEDLE LILOCK LIF ( I ) CAUTERY POLISHER TI P LIF || ( I) SH EET ENT SPLIT 11 0 X 77 || (2) LITE GLOVE || (2) NEEDLE H YPODERM IC 27G X I \!..'' || (1 2) TOWELS CLOTH HUCK (BLUE) || ( I ) TUBE SUCTION CONNECT.'!." X 12' L/F ( I ) EAR ULCER SYRINGE 2oz LIF || ( I ) TABLE COYER REINFORCED 50" X 90" LIF ( I ) UTILITY BOWL 1 6oz LIF || (4) COTrON APPLICATOR 6" WOOD || ( I ) INSTRUMENT WIPE I MM 8.25 X 8.25 || ( I ) MAYO STAND COYER REINFORCED LIF || ( I ) NEEDLE & BLADE COUNTER 20c FOAM/MAG LIF ( I ) SKIN MARK ER W/R ULER || ( I ) SYRINGE IOcc W/0 NEEDLE LILOCK LIF || ( I ) TRAY MAYO SMALL || ( I ) SYRING E IOcc TI P CONTROL LILOCK LIF || ( I ) DRAPE MICROSCOPE ZEI SS || ( I ) TOWELS ABSORBENT 1 5'' X 20" LIF || ( I ) TIME OUT BEACON NON WOV EN ST LIF || ( I ) BLADE M INUATURE CARBON STEEL || ( I 0) GAUZE SPONGE 4" X 4" 1 6PLY XRD LIF || ( I ) NEEDLE BLUNT FI LL 1 80 X I Y, || (2) SCALPEL SAFETY WEIGHTED # 1 5 || ( I ) GOWN SURG, I MP ER. M I CROCOOL LG E (2) GOWN XL SURG ICAL MICROCOOL || ( I ) MERLINO SKIN PREP APPLIC. 39ML LIF || ( I ) WRAPPER 24" X 24" || WET SKIN PACK CONTA INING: ( I ) WRAPPER 30" X 30" || ( I ) TRAY 3/COMPARTM ENT || ( I ) PYP SCRUB SOLUTI ON 4oz. BOTrLE || (3) TI P ABSORBENT APPLICATOR STICK SPONGE || (3) TOWELS ABSORBENT 15" X 20" L/F (6) SPONGE WING SMALL LIF || (2) GLOVE MED FREETOUCI-1 VYN I L P/F || (2) COTrON APPLICATOR 6" WOOD || 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