{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85298",
      "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": "Letter",
      "distribution_pattern": "US Nationwide.  Australia, Bermuda, Belgium, Brazil, Canada, Chile, China, Columbia, Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, Norway, Poland, Portugal, Russia, Singapore, Spain, Sweden, UK.",
      "recall_number": "Z-1834-2020",
      "product_description": "VITROS Immunodiagnostic Products TT4 Reagent Pack, Product Code 8744468",
      "product_quantity": "3181",
      "reason_for_recall": "The specified reagent packs exhibit an increase in the frequency of unsuccessful calibrations.",
      "recall_initiation_date": "20200310",
      "center_classification_date": "20200430",
      "termination_date": "20220926",
      "report_date": "20200506",
      "code_info": "UDI: 10758750005147;  Lot Number: 2340"
    }
  ]
}