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-2421-2014
  • 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)
    Product code 900-1936, 22 lots: 110082088 110082207 110102439 110112627 110112928 111010082 111030630 111041100 111051372 111061520 111071785 111113056 111123422 112010103 112041214 112062469 112083415 113109769 131210637 140111090 140312098 140412891
  • 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
    UNIVERSAL PACK - || (1) UTILITY BOWL 16oz. || (1) NEEDLE SPINAL ANEST. 22G X 31!2 || (1) SYRINGE 5cc WITHOUT NEEDLE LUER LOCK LIF || (2) SYRINGE 10ccWITHOUT NEEDLE LUER LOCK LIF || (1) SYRINGE 30cc WITHOUT NEEDLE LUER LOCK LIF || (1) NEEDLE HYPODERMIC 20G X 1 1!2 || (2) GOWN X-LARGE SMS IMPERVIOUS REINFORCED AAMIIII || (1) SPLIT SHEET WITH ADHESIVE 108" X 77" SMS STD LIF || (1) DRAPE % ECONOMY 53" X 77" UF || (2) TOWEL ABSORBENT 15" X 20" UF || (4) DRAPE UTILITY WITH TAPE LIF || (1 0) GAUZE SPONGES 4" X 4" 12PL Y || (4) TOWELS CLOTH HUCK BLUE || (1) TABLE COVER REINFORCED 50" X 90" UF || (1) SCALPEL WITH HANDLE #11 || (3) PK. CLOSURE SKIN W' X 4" STERI STRIP UF || (1) SKIN MARKER WITH RULER || (1) DENTURE CUP 8oz WITH LID || (1) NEEDLE HYPODERMIC 25 X 1 1!2 || (1) STOCKINETTE IMPERVIOUS 14" X 48" || (2) TIP ABSORB. APPLICATOR STICK SPONGE || (1) TRAY ORGANIZER FULL DEEP || (1) TRA 2/COMPARTMENT || (1) RULER L/F || 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