{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Plymouth",
      "address_1": "13700 1st Ave N",
      "reason_for_recall": "Nonin manufactures and sells two 8500 handheld pulse oximeters (Model 8500 with no memory feature and the 8500M which has a memory feature). Some of the devices distributed may not have the correct  pulse oximetry board with the integrated memory feature.",
      "address_2": "",
      "product_quantity": "15 (11 US; 4 OUS)",
      "code_info": "502002091   502002088   502002087   502002083   502002085   502002086  502002081   502002082   502002080   502002079   502002077   502002078   502002089  502002090",
      "center_classification_date": "20170328",
      "distribution_pattern": "Distribution in US (MI, NC, OH, NC, VA), and CANADA",
      "state": "MN",
      "product_description": "8500M Handheld Pulse Oximeter",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nonin Medical, Inc",
      "recall_number": "Z-1690-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75424",
      "termination_date": "20180312",
      "more_code_info": "",
      "recall_initiation_date": "20160929",
      "postal_code": "55441-4595",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}