{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Athens",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75213",
      "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": "Worldwide Distribution -- US, to the states of TN and MS; and the country of Canada.",
      "recall_number": "Z-0051-2017",
      "product_description": "MicroStic Plus w/SS Wire 5F and MicroStic Plus w/NiTi Wire & Echo Needle 4F.    A sheath used to facilitate placing a catheter through the skin into a vein or artery.",
      "product_quantity": "200 units",
      "reason_for_recall": "The supplier initiated a recall because affected lots of the micro-introducer have an outer diameter of the dilator hub that is slightly smaller than is capable of securing the dilator to the sheath",
      "recall_initiation_date": "20160908",
      "center_classification_date": "20161006",
      "termination_date": "20170607",
      "report_date": "20161012",
      "code_info": "11149662, 11151447, 11151617, and 11149822."
    }
  ]
}