{
  "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": "Terminated",
      "city": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83322",
      "recalling_firm": "Ortho Clinical Diagnostics",
      "address_1": "100 Indigo Creek Dr",
      "address_2": "N/A",
      "postal_code": "14626-5101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide distribution.  US nationwide including Puerto Rico, Brazil, Canada, Chile, France, India, and Philippines.",
      "recall_number": "Z-2180-2019",
      "product_description": "VITROS 5600 Integrated System, clinical chemistry analyzer",
      "product_quantity": "89",
      "reason_for_recall": "Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System",
      "recall_initiation_date": "20190708",
      "center_classification_date": "20190806",
      "termination_date": "20231019",
      "report_date": "20190814",
      "code_info": "product code: 6802915  UDI: 10758750007110  Affected software : Version 3.3.2 or above"
    }
  ]
}