{
  "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-1761-2018",
      "product_description": "POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362",
      "product_quantity": "2395 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)  REAN0058 (01)00801741110740(17)170628(10)REAN0058  REAN0205 (01)00801741110740(17)170628(10)REAN0205  REAN1124 (01)00801741110740(17)170628(10)REAN1124  REAP0769 (01)00801741110740(17)170728(10)REAP0769  REAT1312 (01)00801741110740(17)171128(10)REAT1312  REBP1357 (01)00801741110740(17)180131(10)REBP1357  REBR0999 (01)00801741110740(17)180731(10)REBR0999  REBV0758 (01)00801741110740(17)180930(10)REBV0758"
    }
  ]
}