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-2517-2014
  • 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 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 900-3025, 1 lot: 131110114
  • 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
    Chole Cystectomy All Endo System , code 900-3025, contains: || (1) TABLE COVER 44X 90 UF || (1) SYRINGE 20ccW/O NDL LUER LOCK LIF || (2) MAYO STAND COVER REINFORCED UF || (1) NEEDLE HYPODERMIC || (6) ABSORBENT TOWEL 15 X 20 UF || (1) NEEDLE HYPODERMIC 22G X 1Y. UF || (4) UTILITY DRAPE WIT APE UF || (1) TROCAR DILATING XCELL 5MM X 100 || (3) GOWN XL SURGICAL MICROCOOL L/F || (1) TROCAR ENDOPATH XCEL DILATING TIP || (1) WRAPPER 24" X 24" UF || (1) TUBING INSUFFLATING OPEN TIP W/0 VENT UF || (1) DRAPE LAP ABDO. W/POUCH 102 X 122 X 78 STD UF || (5) APPLICATOR COTTON 6 WOOD UF || (1) ULTRA VERES NEEDLE 120MM LIF || (1) APPLIER MUL Tl CLIP W/SHAF GUN || (1) SPECIMEN CONTAINER 4oz. W/LID & LABEL UF || (2) DRAPE :Y. ECONOMY 53" X 77" UF || (2) UTLITY BOWL 16oz. UF || (1) SCALPEL WEIGHTED SAFETY #11 UF || (1) RING BASIN || (1) TIME OUT BEACON NON WOVEN UF || (1) TUBE SUCTION CONNECT || (1) MERLING SKIN PREP APPLIC 39ML UF || (1 0) GAUZE SPONGE 4 X 4 16PL Y XRD LIF || (2) TOWEL CLOTH HUCK (BLUE) UF || (1 0) GAUZE SPONGE 4 X 4 16PL Y UF || (1) SCISSOR CURVED W/MONOPOLAR CAUTERY 5MM || (5) LAP SPONGE PRE-WASH 18" X 18" XRD UF || (1) DISSECTOR CURVED W/MONOPLAR CAUTERY 5MM || (1) SKIN MARKER INK W/8 LABEUTIMEOUT/RULER LIF || (2) LIGHT SHIELD UF || (1) SUTURE BAG FLORAL UF (4) DRESSING ISLAND 4 X 6 || (1) DRAPE LASER CAMERA W/ELASTIC 6X 96 || (1) PK. STERI STRIP CLOSURE || (1) NEEDLE & BLADE COUNT 60C FOAM STR/MAG STR UF || (1) MAYO TRAY SMALL || (1) SYRINGE 30ML SLIP TIP 1 ML UF || 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