{
  "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": "Ongoing",
      "city": "Buffalo Grove",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84301",
      "recalling_firm": "Leica Microsystems, Inc.",
      "address_1": "1700 Leider Ln",
      "address_2": "N/A",
      "postal_code": "60089-6622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and OUS to Canada.",
      "recall_number": "Z-0673-2020",
      "product_description": "BOND Polymer Refine Detection Kit, Catalog No. DS9800.  This detection system is for in vitro diagnostic use.  Bond Polymer Refine Detection is a biotin-free, polymeric horseradish peroxidase (HRP)-linker antibody conjugate system for the detection of tissue-bound mouse and rabbit IgG and some mouse IgM primary antibodies.  It is intended for staining sections of formalin-fixed, paraffin-embedded tissue on the BOND automated system.",
      "product_quantity": "558",
      "reason_for_recall": "BOND Polymer Refine Detection kits (DS9800) were held out of refrigerated storage longer than specified which may exhibit suboptimal staining.",
      "recall_initiation_date": "20191118",
      "center_classification_date": "20191212",
      "report_date": "20191218",
      "code_info": "Lot:  65549",
      "more_code_info": ""
    }
  ]
}