{
  "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": "Norderstedt",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96386",
      "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": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AL, CA, CO, FL, GA, IN, KS, MO, NJ, NV, OH TX, VA, WI and the countries of Germany, Italy, Spain, Switzerland.",
      "recall_number": "Z-1372-2025",
      "product_description": "Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA =  11 mm, Product Code: 880-601/11",
      "product_quantity": "37 units",
      "reason_for_recall": "A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.",
      "recall_initiation_date": "20250214",
      "center_classification_date": "20250317",
      "report_date": "20250326",
      "code_info": "Product Code: 880-601/11; UDI-DI: 04026575443925; Lot Numbers: 1943294, 1943296, 1943297, 2049174."
    }
  ]
}