{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
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  "results": [
    {
      "country": "United States",
      "city": "Cypress",
      "address_1": "11331 Valley View St",
      "reason_for_recall": "After a submission for CLIA database update from Focus Diagnostics to DiaSorin Molecular,the company found that their Legionella IFA device (IF0950) is not 510(k) exempt.",
      "address_2": "",
      "product_quantity": "196 units",
      "code_info": "Unique Device Identifier IF0950: 20816101020045, lot numbers 30244, 30928, 31288, 31642, 32331, 32562, 32850",
      "center_classification_date": "20170327",
      "distribution_pattern": "Product was distributed to three testing laboratories in California, New Jersey and Virginia",
      "state": "CA",
      "product_description": "Legionella IFA (IF0950) intended for qualitatively detecting and semi-quantitating human serum antibodies to Legionella pneumophila.",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Focus Diagnostics Inc",
      "recall_number": "Z-1685-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76619",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20170215",
      "postal_code": "90630-5366",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}