{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Alpharetta",
      "address_1": "5995 Windward Pkwy",
      "reason_for_recall": "The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.",
      "address_2": "",
      "product_quantity": "106",
      "code_info": "Model Number (software version)  8.0.2 & 8.0.1 with RapiDispense",
      "center_classification_date": "20130826",
      "distribution_pattern": "USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.",
      "state": "GA",
      "product_description": "Mc Kesson Anesthesia-Rx  Model Number 8.0.2 & 8.0.1 with RapiDispense    Product Usage:  Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "MCKESSON TECHNOLOGIES INC",
      "recall_number": "Z-2089-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65769",
      "termination_date": "20140619",
      "more_code_info": "",
      "recall_initiation_date": "20130722",
      "postal_code": "30005-4184",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}