{
  "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": "Hertford",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67781",
      "recalling_firm": "Del Mar Reynolds Medical, Ltd.",
      "address_1": "1-2 Harforde Ct., Foxholes",
      "address_2": "Business Park",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution in the states of North Carolina and South Carolina",
      "recall_number": "Z-1442-2014",
      "product_description": "SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed.  This system includes a ventilator.",
      "product_quantity": "16 units distributed in the US",
      "reason_for_recall": "The System may go into a controlled failed state if a series of parameters on the user interface are activated in a specific sequence.",
      "recall_initiation_date": "20140310",
      "center_classification_date": "20140411",
      "termination_date": "20140820",
      "report_date": "20140423",
      "code_info": "SERIAL NUMBERS OF UNITS DISTRIBUTED IN THE US:    ARKN-000011, ARKN-000016,  ARKN-000017, ARKN-000019, ARKN-000020,  ARKN-000021, ARKN-000022, ARKN-000023, ARKN-000024, ARKN-000025, ARKN-000026, ARKN-000027, ARKN-000028, ARKN-000029,  ARKN-000030, and ARKN-000031."
    }
  ]
}