{
  "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": "2026-04-15",
    "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": "74704",
      "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": "Nationwide, Canada",
      "recall_number": "Z-2549-2016",
      "product_description": "Mindray DS USA Inc., Passport Series Patient Monitor intended for monitoring, displaying, reviewing, alarming, and transferring of multiple physiological parameters including ECG (3-lead, 5-lead or 12-lead selectable, arrythmia detection, ST segment analysis, and heart rate (HR), Respiration rate.",
      "product_quantity": "360 units",
      "reason_for_recall": "Mindray has identified a potential leakage issue with the CO2 Module's Dryline II Water Trap used with the Passport Series Patient Monitor.",
      "recall_initiation_date": "20160623",
      "center_classification_date": "20160816",
      "termination_date": "20170328",
      "report_date": "20160824",
      "code_info": "100-00080-00 - Dyrline II Water Trap, Adult  115-020919-00- CO2 Module with Accessory Kit, Adult and Pediatric    Lot #1534, 1537, 1538, 1541, 1545, 1547, 1548, 1602, and 1606"
    }
  ]
}