{
  "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": "2026-04-29",
    "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": "71757",
      "recalling_firm": "Bard Access Systems",
      "address_1": "605 N 5600 W",
      "address_2": "N/A",
      "postal_code": "84116-3738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to domestic and foreign conference attendees.",
      "recall_number": "Z-2808-2015",
      "product_description": "Marketing brochures for the PowerPICC and PowerPICC SOLO catheters",
      "product_quantity": "1811",
      "reason_for_recall": "Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.",
      "recall_initiation_date": "20150720",
      "center_classification_date": "20150923",
      "termination_date": "20170210",
      "report_date": "20150930",
      "code_info": "The brochures were purchased from the vendor on 04/14/2015, Code S120667R0"
    }
  ]
}