{
  "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": "86096",
      "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": "Worldwide distribution - US Nationwide distribution and the countries of Australia, Belgium, Brazil, Canada, Chile, China,   Colombia, Denmark, France, Germany, India, Italy, Japan,   Mexico, Norway, Poland, Portugal, Russia, Singapore, Spain,   Sweden, The Netherlands, United Kingdom.",
      "recall_number": "Z-2879-2020",
      "product_description": "VITROS XT7600 Integrated System, Product code 6844461",
      "product_quantity": "pending",
      "reason_for_recall": "When processing MicroSlides, slides that utilize Slot 18 in the CM rotor may be mis-positioned. As a result, certain VITROS MicroSlides may produce erroneous results.",
      "recall_initiation_date": "20200720",
      "center_classification_date": "20200824",
      "termination_date": "20231218",
      "report_date": "20200902",
      "code_info": "Serial numbers J76000050 - 76000566"
    }
  ]
}