{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68582",
      "recalling_firm": "Mindray DS USA, Inc. dba Mindray North America",
      "address_1": "800 MacArthur Blvd",
      "address_2": "N/A",
      "postal_code": "07430-2001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including the states of Louisiana, New Jersey, Montana, South Carolina and Wyoming.",
      "recall_number": "Z-2059-2014",
      "product_description": "V-Series Patient Monitoring System, Manufactured for Mindray DS USA, Inc.    Used for monitoring of human physiological parameters.     The V-Series Monitor also has the capability of performing IV Drug and Hemodynamic Calculations and interfacing with network devices.",
      "product_quantity": "113 units (57 United States; 56 International)",
      "reason_for_recall": "ECG interpretation feature issues.  False measurements reported when the algorithm cannot determine P wave or QRS axis.  The Median Complex Report displays the representative beat 25% larger than actual signal input.  When a patient date of birth is imported from an external source, the ECG interpretation algorithm uses the default age of 50, and interpretive statements may be incorrect.",
      "recall_initiation_date": "20140519",
      "center_classification_date": "20140716",
      "termination_date": "20170420",
      "report_date": "20140723",
      "code_info": "Part Number (P/N): 0998-00-1800-101 and 0998-00-1800-201 with software version 2.4.1.18 in use with 12-lead ECG Module, P/N:0998-00-1804-01 and 0998-00-1804-02."
    }
  ]
}