Device Recall HemoSense INRatio2

  • Model / Serial
    Product Numbers: 0200431 and 0200432.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution in the US, Germany, Spain and Australia.
  • Product Description
    HemoSense INRatio2 Prothrombin Time Monitor, manufactured by HemoSense Incorporated. || The INRatio2 PT Monitoring System is used for the quantitative measurement of Prothrombin Time (PT) in fresh, capillary whole blood.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    HemoSense Inc, 651 River Oaks Pkwy, San Jose CA 95134-1907
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    USFDA