{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Norderstedt",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92500",
      "recalling_firm": "Waldemar Link GmbH & Co. KG (Mfg Site)",
      "address_1": "Oststr. 4-10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic: AL, GA, IL, IN, KS, NJ, NY, and TX. Foreign: Argentina, Australia, Austria, Brazil, Finland, France, Germany, India, Italy, Spain, and United Kingdom.",
      "recall_number": "Z-2049-2023",
      "product_description": "LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left",
      "product_quantity": "13 units",
      "reason_for_recall": "The firm discovered through customer complaints that device segments may not meet specifications.",
      "recall_initiation_date": "20210318",
      "center_classification_date": "20230630",
      "report_date": "20230705",
      "code_info": "Item No. 15-2979/02; UDI-DI: 04026575328109.",
      "more_code_info": ""
    }
  ]
}