{
  "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": "Pawtucket",
      "state": "RI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83040",
      "recalling_firm": "Bio-Detek, Inc.",
      "address_1": "525 Narragansett Park Dr",
      "address_2": "N/A",
      "postal_code": "02861-4323",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to accounts in AZ, CA, CO, CT, FL, LA, MN, NV, OH, PA, TN, UT, and WY. International distribution to Canada, Germany, France, and Italy.",
      "recall_number": "Z-1945-2019",
      "product_description": "ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)",
      "product_quantity": "1789",
      "reason_for_recall": "Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy.",
      "recall_initiation_date": "20190528",
      "center_classification_date": "20190703",
      "termination_date": "20200601",
      "report_date": "20190710",
      "code_info": "Lots 1719, 1719A, and 1819"
    }
  ]
}