{
  "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": "2026-04-01",
    "results": {
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      "status": "Terminated",
      "city": "Heverlee",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85080",
      "recalling_firm": "Materialise N.V.",
      "address_1": "Technologielaan 15",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1485-2020",
      "product_description": "TRUMATCH Orthognathics - Genioplasty Surgical Kit, Add-on, Catalog Number: SD980.013",
      "product_quantity": "1",
      "reason_for_recall": "Custom surgical kits contain a plate different than indicated by the package labeling.",
      "recall_initiation_date": "20200203",
      "center_classification_date": "20200313",
      "termination_date": "20200320",
      "report_date": "20200325",
      "code_info": "Lot Number: ME19-ZIK-VIK, UDI: (01)05420060380136(10)ME19ZIKVIK",
      "more_code_info": ""
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}