{
  "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": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70338",
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "address_1": "325 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "07430-2002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of GA, MA, NC, NY & PA.",
      "recall_number": "Z-1241-2015",
      "product_description": "LFT v40 Femoral Head; Catalog Number 6260-9-032;   V40 CoCr LFit Head 32mm/-4.    Designed to be assembled onto a femoral hip stem trunnion during surgery for a total hip arthroplasty.",
      "product_quantity": "9 units",
      "reason_for_recall": "Three customer complaints were received for the same batch of V40 LFIT Vitallium femoral heads (part number 6260-9-032, lot 48681201) alleging that the femoral head couldn't be assembled with its corresponding V40 stem trunnion.",
      "recall_initiation_date": "20150203",
      "center_classification_date": "20150303",
      "termination_date": "20170407",
      "report_date": "20150311",
      "code_info": "Lot Code 48681201"
    }
  ]
}