{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Issy les Moulineaux",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80533",
      "recalling_firm": "Withings Sas",
      "address_1": "2 rue Maurice Hartmann",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-2829-2018",
      "product_description": "Nokia BPM+  Wireless Blood Pressure Monitor    Product System, measurement, blood-pressure, non-invasive",
      "product_quantity": "Total 44,000 units (15,139 US/ 28,861 OUS)",
      "reason_for_recall": "Device could not meet the requirements for systolic pressure",
      "recall_initiation_date": "20180611",
      "center_classification_date": "20180816",
      "report_date": "20180822",
      "code_info": "7024260310",
      "more_code_info": ""
    }
  ]
}