{
  "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 III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63094",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-0194-2013",
      "product_description": "Boule Con-Diff Hematology Control 9 vials.    For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.",
      "product_quantity": "690 packs",
      "reason_for_recall": "Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled the Boule Con Diff US Tri Pack (Product part 501-605, Lot #1005-549 and Product part 501-607, Lot #1005-549) which is used for in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments. The recall was imitated due to receipt of customers stating the MCV values and RDW% recovered for Boule",
      "recall_initiation_date": "20100804",
      "center_classification_date": "20121105",
      "termination_date": "20140814",
      "report_date": "20121114",
      "code_info": "Product part 501-607, Lot #1005-549"
    }
  ]
}