{
  "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": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83528",
      "recalling_firm": "OMNIlife science Inc.",
      "address_1": "480 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution to states of: IL, NY, OK, MD, AL, PA, CO, FL, and UT.",
      "recall_number": "Z-2480-2019",
      "product_description": "OMNIlife science, Inc.   ApeX acetabular liner  hip prosthesis component     Serf Dual Mobility Cup Insert Liner 51-28;   Product code: H6-25128",
      "product_quantity": "22 units",
      "reason_for_recall": "Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.",
      "recall_initiation_date": "20190723",
      "center_classification_date": "20190905",
      "termination_date": "20200424",
      "report_date": "20190911",
      "code_info": "LOT # 31740"
    }
  ]
}