{
  "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": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "800 MacArthur Blvd",
      "reason_for_recall": "An issue has been identified with Passport V Monitors invasive blood pressure function (IBP) which may provide an incorrect IBP measurement",
      "address_2": "",
      "product_quantity": "519 units",
      "code_info": "6100F- PA00195  6100F- PA00197  6100F- PA00219  6100F- PA00221  6100F- PA00267  6100F- PA00269  6100F- PA00291  6100F- PA00293",
      "center_classification_date": "20150316",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "Passport V Monitor, Multiparameter Patient Monitor(with Arrhythmia Detection and Alarms)    Intended for intra hospital use under the direct supervision of a licensed healthcare practitioner.",
      "report_date": "20150325",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mindray DS USA, Inc. dba Mindray North America",
      "recall_number": "Z-1280-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70546",
      "termination_date": "20170420",
      "more_code_info": "",
      "recall_initiation_date": "20150123",
      "postal_code": "07430-2001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}