{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74736",
      "recalling_firm": "Resmed Corporation",
      "address_1": "9001 Spectrum Center Blvd",
      "address_2": "N/A",
      "postal_code": "92123-1438",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution",
      "recall_number": "Z-2550-2016",
      "product_description": "Quattro Air FFM MED \u0013 AMER, Product Code: 62702,  full face mask for use with active-exhaust-valve ventilators",
      "product_quantity": "42 units",
      "reason_for_recall": "Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.",
      "recall_initiation_date": "20160712",
      "center_classification_date": "20160816",
      "termination_date": "20160926",
      "report_date": "20160824",
      "code_info": "Lot 1142623"
    }
  ]
}