{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Raynham",
      "address_1": "480 Paramount Dr",
      "reason_for_recall": "Stems missing porous coating on the device.",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "Lot # 33035",
      "center_classification_date": "20191021",
      "distribution_pattern": "OK, IL",
      "state": "MA",
      "product_description": "OMNI Hip System  Model, Catalogue, or Order Number(s): HC-00070    Intended for use as the femoral component of a primary or revision total hip replacement.",
      "report_date": "20191030",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OMNIlife science Inc.",
      "recall_number": "Z-0169-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83844",
      "termination_date": "20200427",
      "more_code_info": "",
      "recall_initiation_date": "20190911",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}