{
  "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": "Dossenheim",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98753",
      "recalling_firm": "Mint Medical GmbH",
      "address_1": "Friedrich-Ebert-Str. 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Germany, Switzerland, Austria, Belgium, Italy, France, Romania, Netherlands, United Kingdom, Spain, Czech Republic, Ireland, Poland;",
      "recall_number": "Z-2068-2026",
      "product_description": "Mint Lesion;  Software Versions: 3.4.0 up to 3.9.5.;",
      "product_quantity": "101 systems",
      "reason_for_recall": "If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while  performing a read, in rare cases some information may be lost or incorrectly linked to other patients.",
      "recall_initiation_date": "20260107",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "Software Versions: 3.4.0 up to 3.9.5. UDI-DI: 04260495880341, 04260495880358, 04260495880365, 04260495880372, 04260495880389, 04260495880396.",
      "more_code_info": ""
    }
  ]
}