{
  "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": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Inner and outer sterile barriers not fully sealed.",
      "address_2": "",
      "product_quantity": "255",
      "code_info": "Lot: 56211103, 56211401, 56211704, 57284004",
      "center_classification_date": "20180309",
      "distribution_pattern": "Distributed in ten (10) states: AR, DE, FL, IL, IN, MI, NJ, OH, TN, and TX; and Canada, Sweden, United Kingdom, France, Spain, Italy, Japan, Romania, Colombia, Netherlands, and Australia.",
      "state": "NJ",
      "product_description": "Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Howmedica Osteonics Corp.",
      "recall_number": "Z-0940-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79038",
      "termination_date": "20200312",
      "more_code_info": "",
      "recall_initiation_date": "20170721",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}