{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Nussloch",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93467",
      "recalling_firm": "LEICA BIOSYSTEMS NUSSLOCH GMBH",
      "address_1": "Heidelberger Str. 17-19",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US, Nationwide",
      "recall_number": "Z-0590-2024",
      "product_description": "Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)",
      "product_quantity": "98 devices",
      "reason_for_recall": "There is an issue regarding poorly processed and/or damaged biopsy tissue specimens on the HistoCore PEGASUS / HistoCore PEGASUS Plus resulting from an incorrect assignment of the carryover value set for created or edited protocols.",
      "recall_initiation_date": "20231120",
      "center_classification_date": "20231219",
      "report_date": "20240501",
      "code_info": "All devices with serial number: G0061-G0701",
      "more_code_info": ""
    }
  ]
}