{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72945",
      "recalling_firm": "Bard Peripheral Vascular Inc",
      "address_1": "1625 W 3rd St",
      "address_2": "N/A",
      "postal_code": "85281-2438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to CA only.",
      "recall_number": "Z-0737-2016",
      "product_description": "Denali Filter-Jugular/Subclavian DL950J  Denali Filter-Femoral Delivery DL950F.   Intravascular filters.",
      "product_quantity": "1,183 units",
      "reason_for_recall": "IFU missing contraindications:   Patients with uncontrolled sepsis and Patients with known hypersensitivity to nickel-titanium alloys.",
      "recall_initiation_date": "20150313",
      "center_classification_date": "20160201",
      "termination_date": "20160201",
      "report_date": "20160210",
      "code_info": "Product Code: DL950J  Lot Number: GFYA3093, GFYC3745, GFYD2734, GFYF3878, GFYF3879, GFYG3877, GFYG3880, GFYI2699    Product Code: DL950F  Lot Number: GFYA3093, GFYC3745, GFYD2734, GFYF3878, GFYF3879, GFYG3877, GFYG3880, GFYI2699",
      "more_code_info": ""
    }
  ]
}