{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Phoenix",
      "state": "AZ",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63174",
      "recalling_firm": "Accutron Inc",
      "address_1": "1733 W Parkside Ln",
      "address_2": "N/A",
      "postal_code": "85027-1382",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0020-2013",
      "product_description": "Newport Portable Package, Model #50000, Serial #   13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 13737, 13738, 13740, 13768, 13770, 13771, 13772, 13784, 13787.        Product Usage:  Portable Analgesia Gas Machine.",
      "product_quantity": "220 units total",
      "reason_for_recall": "Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.",
      "recall_initiation_date": "20120429",
      "center_classification_date": "20121009",
      "termination_date": "20130201",
      "report_date": "20121017",
      "code_info": "Lot # 73656, 74139, 75209, 74689, 75515, 74858."
    }
  ]
}