{
  "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": "67567",
      "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 Nationwide distribution including WA, KY, IL, and IA.",
      "recall_number": "Z-1300-2014",
      "product_description": "PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system.  Product Codes: 1716000, 1716070",
      "product_quantity": "777",
      "reason_for_recall": "Labeling discrepancy.The label states that the implantable port contains silicone suture plugs, however approximately 23% of the units contained in the affected lots have a PowerPort Slim titanium implantable port without silicone suture plugs.",
      "recall_initiation_date": "20140227",
      "center_classification_date": "20140327",
      "termination_date": "20140905",
      "report_date": "20140402",
      "code_info": "Lot Numbers: REXA1302, REXA1350, REXB1160"
    }
  ]
}