{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4412
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Auckland",
      "state": "",
      "country": "New Zealand",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95942",
      "recalling_firm": "Adept Medical Ltd",
      "address_1": "2-6 Mc Donald Street",
      "address_2": "Morningside, Po Box 10075 Dominion Rd",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.  International: Canada, New Zealand, Australia, Yemen, United Kingdom, Spain, Italy, Turkey, El Salvador, Malaysia, United Arab Emirates, Germany, Greece, Syria, Peru, Hong Kong, Turkey, Chile, Ireland.",
      "recall_number": "Z-0966-2025",
      "product_description": "Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;",
      "product_quantity": "6,280 units (2500 US, 3780 OUS)",
      "reason_for_recall": "Lack of 510(k) clearance.",
      "recall_initiation_date": "20241124",
      "center_classification_date": "20250117",
      "report_date": "20250129",
      "code_info": "Product Code: NZ3309; UDI-DI: 09421901970369; Lots: 2008-1459; 2009-1864; 2011-2331, 2012-2961, 2013-3122, 2013-3363, 2014-3783, 2014-3832, 2015-3943, 2016-4601, 2016-5197, 2017-5651, 2017-6150, 2018-6487, 2018-6818, 2019-7211, 2021-10033, 2022-10783, 2023-11053,",
      "more_code_info": ""
    }
  ]
}