{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66223",
      "recalling_firm": "Access Scientific Inc",
      "address_1": "3910 Sorrento Valley Blvd Ste 200",
      "address_2": "N/A",
      "postal_code": "92121-1419",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Distributed in MI and TX.",
      "recall_number": "Z-2254-2013",
      "product_description": "POWERWAND Safety Introducer with Extended Dwell Catheter;  Catalog no. 92006.    Used to gain access to the vascular system to sample blood and administer fluids intravenously.",
      "product_quantity": "160 units",
      "reason_for_recall": "Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is mislabeled.",
      "recall_initiation_date": "20130816",
      "center_classification_date": "20130918",
      "termination_date": "20130924",
      "report_date": "20130925",
      "code_info": "Lot no. I666473",
      "more_code_info": ""
    }
  ]
}