Device Recall Lifescan OneTouch Ultra Meter

  • 모델명 / 제조번호(시리얼번호)
    Includes all System Kits shipped during June 2003 until December 2003
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    The recall product was distributed in the U.S. only. LifeScan manufactured and distributed OneTouch Ultra System Kits with the affected OneTouch Ultra Meter Owner''s Booklets between March 31, 2003 and October 3, 2003.
  • 제품 설명
    LifeScan brand OneTouch Ultra Meter - Owner''s Booklet; || Product is manufactured and distributed by LifeScan, Inc., 1000 Gibraltar Dr., Milpitas, CA 95037
  • Manufacturer
  • 1 Event

제조사

  • 제조사 주소
    Lifescan Inc, 1000 Gibraltar Dr, Milpitas CA 95035-6301
  • Source
    USFDA