{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Borehamwood",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73856",
      "recalling_firm": "Stanmore Implants Worldwide Ltd.",
      "address_1": "210 Centennial Avenue Centennial Park",
      "address_2": "Centennial Park",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to OH.",
      "recall_number": "Z-1623-2016",
      "product_description": "Distal Femoral Replacement (patient specific, custom made orthopedic implant device).  PIN 19960",
      "product_quantity": "1",
      "reason_for_recall": "Incorrect component used to manufacture distal femoral replacement.",
      "recall_initiation_date": "20160412",
      "center_classification_date": "20160509",
      "termination_date": "20170126",
      "report_date": "20160518",
      "code_info": "Device Identifier: PIN 19960, Lot: 19960"
    }
  ]
}