{
  "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": "Borehamwood",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75892",
      "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": "Nationwide Distribution to OH, NE, FL, LA, NY, TX, MS, MD, CT, AL, PA",
      "recall_number": "Z-0822-2017",
      "product_description": "Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm  The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone",
      "product_quantity": "11 units",
      "reason_for_recall": "The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.",
      "recall_initiation_date": "20161207",
      "center_classification_date": "20161219",
      "termination_date": "20170717",
      "report_date": "20161228",
      "code_info": "B10191,  B10443,  B9920,  B10561,  B9921,  B9922"
    }
  ]
}