{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Oakland",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87086",
      "recalling_firm": "Topcon Medical Systems, Inc.",
      "address_1": "111 Bauer Dr",
      "address_2": "",
      "postal_code": "07436-3123",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "AZ, MO, NC, NY, PA, TX",
      "recall_number": "Z-0952-2021",
      "product_description": "Harmony Referral System (aka Harmony RS)/ Medical Device  Data System - Product Usage: intended to be used by trained healthcare professionals and clinicians to access archived multimedia data, forms and patient information.",
      "product_quantity": "13 units",
      "reason_for_recall": "Harmony RS integrations with Topcon equipment, TRC NW-400 and the Signal Camera, allowed user input of non-unique patient IDs that caused multiple patient records and images to be combined under the first generated record",
      "recall_initiation_date": "20201218",
      "center_classification_date": "20210204",
      "termination_date": "20221019",
      "report_date": "20210210",
      "code_info": "Software Version 3.1",
      "more_code_info": ""
    }
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}