{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plantation",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67724",
      "recalling_firm": "Clinical Diagnostic Solutions",
      "address_1": "1800 Nw 65th Ave Ste 2",
      "address_2": "N/A",
      "postal_code": "33313-4544",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution:  USA Nationwide and the countries of IVORY COAST, MEXICO, and Philippines.",
      "recall_number": "Z-1436-2014",
      "product_description": "Boule Con-Diff Tri-Level  Multi-Parameter Assayed Hematology Control, used for in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.",
      "product_quantity": "3,540",
      "reason_for_recall": "Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.",
      "recall_initiation_date": "20130224",
      "center_classification_date": "20140408",
      "termination_date": "20140807",
      "report_date": "20140416",
      "code_info": "Product Part Number:  501-605 Lot# 1311-682 Exp. 3/26/2014  501-607 Lot# 1311-683, 1311-684  Exp. 3/26/2014  501-608 Lot# 1311-683 Exp. 3/26/2014"
    }
  ]
}