{
  "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": "Andover",
      "address_1": "2 Dundee Park Dr",
      "reason_for_recall": "The CO/CO2 sensor cable harness may have lower electromagnetic shielding, which might have resulted in a non-compliance with the IEC 60601-1-2 standard.  As a consequence of a lower electromagnetic shielding provided by the cable harness, the CO/CO2 sensor could have been influenced by high frequencies emitted by very close devices.",
      "address_2": "",
      "product_quantity": "37 total devices",
      "code_info": "Serial Numbers: 550066  550067  550068  550069  550071  550072",
      "center_classification_date": "20191203",
      "distribution_pattern": "The products were distributed to the following US states:  KY, MO, NY, OH, PA",
      "state": "MA",
      "product_description": "EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1",
      "report_date": "20191211",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "NDDd Medical Technologies, Inc.",
      "recall_number": "Z-0596-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "83992",
      "termination_date": "20200505",
      "more_code_info": "",
      "recall_initiation_date": "20170815",
      "postal_code": "01810-3735",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}