{
  "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-1760-2018",
      "product_description": "POWERPORT(R) ClearVUE(R) isp with Smooth Septum, 6F ChronoFlex(TM), Polyurethane Catheter, REF 1666362",
      "product_quantity": "359 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)  REAN0063 (01)00801741110726(17)170628(10)REAN0063  REAN1123 (01)00801741110726(17)170628(10)REAN1123  REAP0467 (01)00801741110726(17)170728(10)REAP0467  REAY1733 (01)00801741110726(17)180331(10)REAY1733  REBS1266 (01)00801741110726(17)180731(10)REBS1266  REBV1731 (01)00801741110726(17)181231(10)REBV1731  REBX1626 (01)00801741110726(17)190331(10)REBX1626  REBY0777 (01)00801741110726(17)190430(10)REBY0777"
    }
  ]
}