{
  "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": "Bettlach",
      "state": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94040",
      "recalling_firm": "Thommen Medical AG",
      "address_1": "Eschenweg 3",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of OH and KY.",
      "recall_number": "Z-1322-2024",
      "product_description": "impression coping, repositionable, short, screw-retained, PF 4.0",
      "product_quantity": "20 units",
      "reason_for_recall": "The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.",
      "recall_initiation_date": "20240124",
      "center_classification_date": "20240320",
      "report_date": "20240327",
      "code_info": "Article No. 3.03.079; UDI/DI: 07640156475463; Lot No. 30972.",
      "more_code_info": ""
    }
  ]
}