{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69683",
      "recalling_firm": "Bard Access Systems",
      "address_1": "605 North 5600 West",
      "address_2": "N/A",
      "postal_code": "84116-3738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to state of: TX, OK, LA, and AR.",
      "recall_number": "Z-0493-2015",
      "product_description": "GuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer: Bard Access Systems, Inc. USA. Product Code FP23AD006.",
      "product_quantity": "2532 units",
      "reason_for_recall": "Bard Access Systems is recalling GuardIVa (Ref. No. FP23AD006) from lot ASXHT003 because they were non-sterile unit samples which potentially could be used clinically.",
      "recall_initiation_date": "20141103",
      "center_classification_date": "20141201",
      "termination_date": "20150512",
      "report_date": "20141210",
      "code_info": "Product Code FP23AD006, Lot No.ASXHT003, Expiration  Date Feb 2016"
    }
  ]
}