{
  "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": "Pacheco",
      "address_1": "60 Berry Dr",
      "reason_for_recall": "Chromogen failed to develop due to a stability issue caused by environmental factors with a raw material in the Vulcan Fast Red Buffer.",
      "address_2": "",
      "product_quantity": "43 units",
      "code_info": "Lot numbers 011818 and 022818",
      "center_classification_date": "20180705",
      "distribution_pattern": "CA, VT, KY, LA, OR, RI, GA, IL, MA, TX, KS, FL, Japan, and Germany",
      "state": "CA",
      "product_description": "Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP) detection system. Catalog numbers FR805-5L and FR805S",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biocare Medical, LLC",
      "recall_number": "Z-2360-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80322",
      "termination_date": "20200714",
      "more_code_info": "",
      "recall_initiation_date": "20180424",
      "postal_code": "94553-5601",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}