{
  "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": [
    {
      "country": "United States",
      "city": "Tempe",
      "address_1": "1625 W 3rd St Bldg 1",
      "reason_for_recall": "Device is at risk of having detectable levels of bacterial endotoxin present on the packaging hoop that the catheter is packaged in. The bacterial endotoxin levels for the catheters are within acceptable levels; however, if bacterial endotoxins are present on the packaging hoops it may have the potential for cross-contamination in a clinical setting.",
      "address_2": "",
      "product_quantity": "140 units",
      "code_info": "UDI: (01)00801741067921(17)191115(10)VTBY0563, Lot Number: VTBY0563",
      "center_classification_date": "20180511",
      "distribution_pattern": "Nationwide Distribution",
      "state": "AZ",
      "product_description": "BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter, 0.035\", 150 cm, REF SK15035M.    Intended to support a guidewire during access into the vasculature.",
      "report_date": "20180523",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "recall_number": "Z-1802-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79896",
      "termination_date": "20210302",
      "more_code_info": "",
      "recall_initiation_date": "20180416",
      "postal_code": "85281-2438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}