{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Freiburg Im Breisgau",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91479",
      "recalling_firm": "Stryker Leibinger GmbH & Co. KG",
      "address_1": "Botzinger Str. 41",
      "address_2": "",
      "postal_code": "N/A",
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      "initial_firm_notification": "E-Mail",
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      "recall_number": "Z-1234-2023",
      "product_description": "Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis",
      "product_quantity": "1 unit",
      "reason_for_recall": "Device was shipped without having regulatory approval.",
      "recall_initiation_date": "20221206",
      "center_classification_date": "20230307",
      "report_date": "20230315",
      "code_info": "TMJ Reconstruction Prosthesis, Catalog #2208151054, Lot Number W67725  UDI/DI: B004YYMMDDNNNNLM0",
      "more_code_info": ""
    }
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}