{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "167177",
      "product_res_number": "Z-0019-2019",
      "event_date_initiated": "2018-09-04",
      "event_date_created": "2018-10-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-07-10",
      "res_event_number": "80986",
      "product_code": "KIM",
      "product_description": "Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.",
      "code_info": "Serial Number  102",
      "firm_fei_number": "3000210133",
      "recalling_firm": "Leica Microsystems, Inc.",
      "address_1": "1700 Leider Ln",
      "city": "Buffalo Grove",
      "state": "IL",
      "postal_code": "60089-6622",
      "additional_info_contact": "Adam Blunier\n847-821-3462",
      "reason_for_recall": "Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock.",
      "root_cause_description": "Process design",
      "action": "The firm issued a Field Action Notice by letter on 09/05/2018.  The notice explained the issue and the possible hazard.  The firm will schedule a visit with a service engineer to perform the correction.",
      "product_quantity": "1 unit",
      "distribution_pattern": "Distribution in US state of MO.",
      "openfda": {
        "registration_number": [
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          "2083544",
          "3015167933",
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          "3003584784",
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        ],
        "device_name": "Device For Sealing Microsections",
        "medical_specialty_description": "Pathology",
        "regulation_number": "864.3400",
        "device_class": "1",
        "k_number": [
          "K780261"
        ]
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}