{
  "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": "Redmond",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72953",
      "recalling_firm": "Fukuda Denshi USA, Inc.",
      "address_1": "17725 NE 65th St Ste C",
      "address_2": "N/A",
      "postal_code": "98052-4911",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of CO, ID, KS, MI, MO, OR, PA, TX, UT, and WI.",
      "recall_number": "Z-0661-2016",
      "product_description": "Fukuda Denshi patient monitor model DS-8100M and DS-8100N.    The Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Monitor is  meant to acquire and monitor physiological signals from patients.",
      "product_quantity": "95 units distributed in the US",
      "reason_for_recall": "A possible malfunction where a Short-term Battery Error message has appeared and has been traced back to a bad (damaged) Lithium-Ion capacitor (Short-term Backup battery).",
      "recall_initiation_date": "20151221",
      "center_classification_date": "20160115",
      "termination_date": "20160819",
      "report_date": "20160127",
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      "more_code_info": ""
    }
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}