{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89072",
      "recalling_firm": "Cook Inc.",
      "address_1": "750 N Daniels Way",
      "address_2": "",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "AL, AZ, CA, FL, GA, KS, MI, MO, MN, NC, NY, OK, TX Foreign: BE, CH, DE, ES, FR, GB,GU, IT, ZA",
      "recall_number": "Z-0388-2022",
      "product_description": "Flexor Check-Flo Introducer Ansel Modification  Model Number: KCFW-7.0-18/38-45-RB-ANL0-HC Order Number/GPN: G44155  Intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.",
      "product_quantity": "47 units",
      "reason_for_recall": "Flexor Check-Flo Introducer Ansel Modification  mislabeled. Products packaged with a label stating 6FR may contain a 7FR device and vice versa",
      "recall_initiation_date": "20211112",
      "center_classification_date": "20211216",
      "termination_date": "20240426",
      "report_date": "20211222",
      "code_info": "Lot Number: 13911710 UDI: (01)00827002441552(17)240422(10)13911710",
      "more_code_info": ""
    }
  ]
}