{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79841",
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "address_1": "1625 W 3rd St Bldg 1",
      "address_2": "N/A",
      "postal_code": "85281-2438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1763-2018",
      "product_description": "POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1676301",
      "product_quantity": "216 units",
      "reason_for_recall": "The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.",
      "recall_initiation_date": "20180208",
      "center_classification_date": "20180509",
      "report_date": "20180516",
      "code_info": "Lot Number Unique Device Identifier (UDI)  REAN0065 (01)00801741110788(17)170628(10)REAN0065  REAP0473 (01)00801741110788(17)170728(10)REAP0473  REAX1813 (01)00801741110788(17)180430(10)REAX1813  REAZ0278 (01)00801741110788(17)180331(10)REAZ0278  REBS1438 (01)00801741110788(17)180930(10)REBS1438  REBT1881 (01)00801741110788(17)180930(10)REBT1881"
    }
  ]
}