{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Norderstedt",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81762",
      "recalling_firm": "Waldemar Link GmbH & Co. KG (Mfg Site)",
      "address_1": "Oststr. 4-10",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution to states of: AZ, FL, GA, LA, MI, MN, TX, and WA.",
      "recall_number": "Z-0728-2019",
      "product_description": "BiMobile UHMWPE Liner: ID-28mm/OD-50mm, Reference Number 184-260/02    The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intended for cemented and cementless use.",
      "product_quantity": "30",
      "reason_for_recall": "The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records.",
      "recall_initiation_date": "20181204",
      "center_classification_date": "20190111",
      "termination_date": "20200605",
      "report_date": "20190123",
      "code_info": "Lot# 1707121",
      "more_code_info": ""
    }
  ]
}