{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Richmond",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87616",
      "recalling_firm": "CHANGE HEALTHCARE CANADA COMPANY",
      "address_1": "10711 Cambie Rd Suite 130",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic Distribution only. IN, KY, CA, NY, WA, IL, IA, FL, TX, WA, MI, HI, AK, WI, WY, NE, AZ, OH, PA",
      "recall_number": "Z-1508-2021",
      "product_description": "Change Healthcare Enterprise Viewer",
      "product_quantity": "28 units",
      "reason_for_recall": "Change Healthcare has identified an intermittent software defect which may result in an anchor study failing to display.",
      "recall_initiation_date": "20210317",
      "center_classification_date": "20210428",
      "report_date": "20210505",
      "code_info": "Change Healthcare Enterprise Viewer 2.0 and 2.1",
      "more_code_info": ""
    }
  ]
}