{
  "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": "Durham",
      "address_1": "300 West Morgan St",
      "reason_for_recall": "There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case.",
      "address_2": "STE 200",
      "product_quantity": "10",
      "code_info": "MAC 14.3.1/MAC 14.3.1.1",
      "center_classification_date": "20140305",
      "distribution_pattern": "Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA.",
      "state": "NC",
      "product_description": "McKesson Anesthesia Care    Product Usage:  The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.",
      "report_date": "20140312",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "MCKESSON TECHNOLOGIES INC.",
      "recall_number": "Z-1060-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "66287",
      "termination_date": "20140501",
      "more_code_info": "",
      "recall_initiation_date": "20130315",
      "postal_code": "27701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}