{
  "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": [
    {
      "status": "Ongoing",
      "city": "Athens",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89439",
      "recalling_firm": "Argon Medical Devices, Inc",
      "address_1": "1445 Flat Creek Rd",
      "address_2": "N/A",
      "postal_code": "75751-5002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV, OH, TX, VA, TN.",
      "recall_number": "Z-0563-2022",
      "product_description": "1. Arterial Line Kit 20ga x 6\"    2. Arterial Line Kit /1 20ga x 6\"",
      "product_quantity": "600 ea",
      "reason_for_recall": "Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss.",
      "recall_initiation_date": "20220124",
      "center_classification_date": "20220204",
      "report_date": "20220216",
      "code_info": "1. Model: 400115A and Serial # 11377499, Expire Date: 10/27/2022    2. Model: 498100 and Serial # 11378381, Expire Date: 4/15/2026"
    }
  ]
}