{
  "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": "2026-04-15",
    "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": "75936",
      "recalling_firm": "Ortho-Clinical Diagnostics",
      "address_1": "513 Technology Blvd",
      "address_2": "N/A",
      "postal_code": "14626-3601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - Nationwide U.S.A; International - Bermuda, Australia, Canada, Chile, China, Colombia, India, Japan, Mexico, Republic of Panama, Singapore, Venezuela, England, France, Germany, Italy, Spain and Poland.",
      "recall_number": "Z-1179-2017",
      "product_description": "VITROS Chemistry Products UPRO Slides, UPN 10758750000593,       Product Usage:  Quantitative measurement of total protein concentration in urine.",
      "product_quantity": "37,571 packs/90 slides totalling 3,381,390 slides",
      "reason_for_recall": "There is a potential for variable negatively and positively biased urine protein results using VITROS UPRO Slides.",
      "recall_initiation_date": "20161208",
      "center_classification_date": "20170209",
      "termination_date": "20180622",
      "report_date": "20170215",
      "code_info": "Product Code REF 680 0120  Lot: GENs 14-18    Expiry Date range 01-JAN-2017 through 01-MAY-2018"
    }
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}