{
  "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": "Ongoing",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85475",
      "recalling_firm": "Immersivetouch Inc",
      "address_1": "910 W Van Buren St Ste 715",
      "address_2": "N/A",
      "postal_code": "60607-3573",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "The device was distributed in the state of Illinois only.",
      "recall_number": "Z-2041-2020",
      "product_description": "ImmersiveView software version 2.1    Product Usage:  ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options",
      "product_quantity": "2 units",
      "reason_for_recall": "Observed an internal repetitive software glitch in ImmersiveView.",
      "recall_initiation_date": "20200403",
      "center_classification_date": "20200518",
      "report_date": "20200527",
      "code_info": "V 2.1"
    }
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}