{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mechelen",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96022",
      "recalling_firm": "Biocartis Nv",
      "address_1": "B 3",
      "address_2": "Generaal De Wittelaan 11",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US:  AL, NJ, TX, OH, CA",
      "recall_number": "Z-0836-2025",
      "product_description": "Idylla INSTRUMENT, IVD, REF P0010.  Intended for the detection of nucleic acid targets in various types of human samples, using disposable Test-specific ldylla Cartridges.",
      "product_quantity": "8 units",
      "reason_for_recall": "False-positive MSI-H results generated by the Idylla MSI Test.",
      "recall_initiation_date": "20241210",
      "center_classification_date": "20250110",
      "report_date": "20250122",
      "code_info": "UDI/DI 05415219000119, Serial Numbers:  00002706, 00002820, 00003103, 00003262, 00003419, 00003434, 00003444, and 00003445.",
      "more_code_info": ""
    }
  ]
}