{
  "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": [
    {
      "country": "United States",
      "city": "Buffalo Grove",
      "address_1": "1700 Leider Ln",
      "reason_for_recall": "The staining intensity decreases over the shelf life.",
      "address_2": "",
      "product_quantity": "309 units",
      "code_info": "Product Code: NCL-L-CD15; Lot Numbers and Expiration Dates: Lot 6022274, Expiry 2015-04; Lot 6024628, Expiry 2015-08; Lot 6030581, Expiry 2016-07",
      "center_classification_date": "20150324",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of CA, CT, FL, IA, ID, IL, MT, NC, NY, TX, WA and in the countries of:  Argentina, Australia, Bosnia and Herzegovina, Brazil, Canada, Chile, Denmark, El Salvador, France, Germany, Hungary, India, Italy, Japan, Netherlands, Nigeria, Portugal, Romania, Russia, Saudi Arabia, Serbia, South Africa, Spain, Sweden, Switzerland, Taiwan, Tunisia, Turkey, United Arab Emirates, United Kingdom.",
      "state": "IL",
      "product_description": "Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform immunohistochemical (IHC) staining.    Product Usage: NCL-L-CD15 is intended for the qualitative identification by light microscopy of CD15 molecules in paraffin sections. The clinical interpretation of any staining or its absence should be complemented by morphological studies using proper controls and should be evaluated within the context of the patient\u0019s clinical history and other diagnostic tests by a qualified pathologist.",
      "report_date": "20150401",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Leica Microsystems, Inc.",
      "recall_number": "Z-1315-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70090",
      "termination_date": "20170905",
      "more_code_info": "",
      "recall_initiation_date": "20141216",
      "postal_code": "60089-6622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}