Device Recall Legionella IFA

  • Model / Serial
    Unique Device Identifier IF0950: 20816101020045, lot numbers 30244, 30928, 31288, 31642, 32331, 32562, 32850
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Product was distributed to three testing laboratories in California, New Jersey and Virginia
  • Product Description
    Legionella IFA (IF0950) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Focus Diagnostics Inc, 11331 Valley View St, Cypress CA 90630-5366
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    IF0951: 10816101020055, lot numbers 29428, 31871
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Product was distributed to three testing laboratories in California, New Jersey and Virginia
  • Product Description
    Legionella IFA Substrate Slide (IF0951) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila.
  • Manufacturer