{
  "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-2185-2019",
      "product_description": "VITROS Chemistry Products Calibrator Kit 32, for use with VITROS clinical chemistry analyzer",
      "product_quantity": "N/A",
      "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:6844508  UDI: 10758750032105  Affected Assay Data Disk (ADD) DRV No: DRV 6032 or above"
    }
  ]
}