{
  "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-2176-2019",
      "product_description": "VITROS 250AT Chemistry System, clinical chemistry analyzer",
      "product_quantity": "30",
      "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: 1758143  UDI: 10758750000036  Affected software : Version 9.7"
    }
  ]
}