{
  "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": [
    {
      "status": "Terminated",
      "city": "Tampa",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83173",
      "recalling_firm": "Cardiocommand Inc.",
      "address_1": "4920 W Cypress St Ste 110",
      "address_2": "N/A",
      "postal_code": "33607-3837",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States - AR, NM, PA, TX, and WA.",
      "recall_number": "Z-1976-2019",
      "product_description": "TAPSYSTEM Model 2A, REF 8002A",
      "product_quantity": "6 units",
      "reason_for_recall": "There is a potential for an assembly error resulting in the battery wire being connected to the ON/OFF power switch incorrectly.",
      "recall_initiation_date": "20190624",
      "center_classification_date": "20190715",
      "termination_date": "20210401",
      "report_date": "20190724",
      "code_info": "SERIAL NUMBERS: 2197A, 2196A, 2198A, 2199A, 2200A, and 2201A,"
    }
  ]
}