{
  "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-1766-2018",
      "product_description": "POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362",
      "product_quantity": "876 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)  REAN0067 (01)00801741110825(17)170628(10)REAN0067  REAP0630 (01)00801741110825(17)170728(10)REAP0630  REAS2309 (01)00801741110825(17)171028(10)REAS2309  REAV2088 (01)00801741110825(17)171028(10)REAV2088  REAY0330 (01)00801741110825(17)171031(10)REAY0330  REBS1275 (01)00801741110825(17)180731(10)REBS1275  REBT1568 (01)00801741110825(17)181031(10)REBT1568  REBV0713 (01)00801741110825(17)181231(10)REBV0713"
    }
  ]
}