{
  "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": "Blue Ash",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89193",
      "recalling_firm": "Gentherm Medical, LLC",
      "address_1": "12011 Mosteller Rd Fl 3",
      "address_2": "N/A",
      "postal_code": "45241-1528",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Chile, Hong Kong, Korea, UAE.",
      "recall_number": "Z-0496-2022",
      "product_description": "Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193",
      "product_quantity": "484 devices",
      "reason_for_recall": "This recall has been initiated to provide a labeling update with revised instruction how to operate the unit with Cold Therapy pads.",
      "recall_initiation_date": "20211122",
      "center_classification_date": "20220113",
      "termination_date": "20230508",
      "report_date": "20220119",
      "code_info": "UDI- 10613031861938;  Affected Serial Numbers are: (164-76703084 Through 213-76703694)"
    }
  ]
}