{
  "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": "2015-01-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Milwaukee",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98649",
      "recalling_firm": "Diversatek Healthcare",
      "address_1": "102 E Keefe Ave",
      "address_2": "N/A",
      "postal_code": "53212-1535",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  MO, CA, FL, TX, AZ, PA, RI, NC, IL, MS, KS, NY, OH, VA, LA, IA, MI, NJ, AL, Brazil, Belgium",
      "recall_number": "Z-1940-2026",
      "product_description": "Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18",
      "product_quantity": "250 units",
      "reason_for_recall": "The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.",
      "recall_initiation_date": "20260318",
      "center_classification_date": "20260423",
      "report_date": "20260429",
      "code_info": "UDI/DI 00816734021798, Lot Numbers:  005985",
      "more_code_info": ""
    }
  ]
}