{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "College Station",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93446",
      "recalling_firm": "CardioQuip, LLC",
      "address_1": "8422 Calibration Ct",
      "address_2": "N/A",
      "postal_code": "77845-5328",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: California, Texas, Pennsylvania, Washington, Ohio, Nebraska OUS: None",
      "recall_number": "Z-0566-2024",
      "product_description": "CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A",
      "product_quantity": "2 units",
      "reason_for_recall": "There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.",
      "recall_initiation_date": "20231024",
      "center_classification_date": "20231215",
      "report_date": "20231227",
      "code_info": "UDI: 00860000846110 /Lot #:11160294 and 11161110"
    }
  ]
}