{
  "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": "82561",
      "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 in the states of AZ, CA, IL, OH, FL, TX, MI  Foreign:  Australia, Belgium, Chile, India, Italy, Japan, South Korea, Spain, Canada,, Phillippines",
      "recall_number": "Z-1364-2019",
      "product_description": "VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW  Product Code: 6844461    Product Usage:  INTENDED USE: For in vitro diagnostic use only. The VITROS XT 7600 Integrated System is intended for use in the measurement of a variety of analytes of clinical interest",
      "product_quantity": "85 units: US=19;OUS=66",
      "reason_for_recall": "Potential for sample fluid to be dispensed to an incorrect position on the MicroSlide, potentially leading to erroneous assay results being reported",
      "recall_initiation_date": "20190320",
      "center_classification_date": "20190520",
      "termination_date": "20201208",
      "report_date": "20190529",
      "code_info": "Serial Number 76000108 thru current."
    }
  ]
}