{
  "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": "British Columbia",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85068",
      "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": "Distribution US nationwide, Canada and the United Kingdom",
      "recall_number": "Z-1682-2020",
      "product_description": "McKesson Cardiology ECG Management, Change Healthcare Cardiology ECG Management",
      "product_quantity": "51 units",
      "reason_for_recall": "Inaccurate estimation of the heart rate may occur in instances where the user is estimating heart rate counting grid squares using the Sequential ECG format",
      "recall_initiation_date": "20200210",
      "center_classification_date": "20200408",
      "report_date": "20200415",
      "code_info": "McKesson Cardiology Software Versions: 13.2.1 HF1, 13.2.1 HF2, 14.0, 14.0 HF1, 14.0 HF2;      Change Healthcare Software Versions: 14.1.1, 14.2"
    }
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}