{
  "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": "Acetabular Liners have a higher than acceptable oxidation limit, potential for patients to experience a higher wear rate for acetabular liners and require a  revision surgery",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "Lot Number: 28413",
      "center_classification_date": "20210126",
      "distribution_pattern": "AL, ID, MD, NY, OK",
      "state": "MA",
      "product_description": "SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures.  Product Code: H6-25128",
      "report_date": "20210203",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OMNIlife science Inc.",
      "recall_number": "Z-0920-2021",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "87062",
      "termination_date": "20210610",
      "more_code_info": "",
      "recall_initiation_date": "20201221",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}