{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Mahwah",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99828",
      "recalling_firm": "Mindray DS USA, Inc.",
      "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 - Nationwide and the country of Canada.",
      "recall_number": "Z-0110-2027",
      "product_description": "BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.",
      "product_quantity": "44,651 units",
      "reason_for_recall": "Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions",
      "recall_initiation_date": "20260831",
      "center_classification_date": "20261007",
      "report_date": "20261014",
      "code_info": "Part numbers of BeneVision N1 and N-Series Patient Monitors Operator's Manuals: 1. BeneVision N1 Operator's Manual up to and including revision 21.0; Part No. 046-011405-00.  2. BeneVision N-Series Operator's Manual up to and including revision 23; Part No. 046-011259-0."
    }
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}