{
  "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": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire",
      "address_2": "",
      "product_quantity": "20 units",
      "code_info": "Lot Number: 53778501  UDIs: (01)04546540035806(17)201108(10)53778501",
      "center_classification_date": "20200115",
      "distribution_pattern": "CA, FL, GA , IA, MA, MI, NC, OH, WI  Foreign: Canada, Japan",
      "state": "NJ",
      "product_description": "Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum   Catalog #:  2041C-3254",
      "report_date": "20200122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Howmedica Osteonics Corp.",
      "recall_number": "Z-0811-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84346",
      "termination_date": "20200831",
      "more_code_info": "",
      "recall_initiation_date": "20191107",
      "postal_code": "07430-2006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}