{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "48611",
      "product_res_number": "Z-0073-2007",
      "event_date_initiated": "2006-08-29",
      "event_date_posted": "2006-10-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-01-28",
      "res_event_number": "36413",
      "product_code": "JBD",
      "k_numbers": [
        "K991362"
      ],
      "product_description": "HYDRAGEL 15 Alkaline Hemoglobin (E) kit, in vitro diagnostic, Sebia Parc Technologique Leonard de Vinci, Rue Leonard de Vinci, 91090 Lisses, France",
      "code_info": "Cat. Number 4126, Lot numbers: 22026/01, 14036/01, 12066/02 and 12066/03.",
      "firm_fei_number": "3001595416",
      "recalling_firm": "Sebia,  Inc.",
      "address_1": "400-1705 Corporate Dr.",
      "city": "Norcross",
      "state": "GA",
      "postal_code": "30093",
      "additional_info_contact": "Karen Anderson\n770-446-3707 Ext. 3704",
      "reason_for_recall": "The material used in packaging the product results in the presence of an additional artifact band above the HbA fraction.",
      "root_cause_description": "Other",
      "action": "Consignees were notified via fax letter and also by phone contact on or about 08/29/2006.",
      "product_quantity": "71 kits",
      "distribution_pattern": "Nationwide (AL, CA, CO, FL, GA, IL, KA, LA, MD, MI, NM, NC, NJ, NY, PA, TX, VA, WI) and Puerto Rico",
      "openfda": {
        "k_number": [
          "K780163",
          "K991362",
          "K800854",
          "K802884",
          "K830804",
          "K901143",
          "K800853",
          "K800855",
          "K802821",
          "K771649",
          "K931503",
          "K982426",
          "K810047",
          "K053571",
          "K813395",
          "K800856",
          "K791008",
          "K820518",
          "K781119",
          "K810919",
          "K931465",
          "K032862",
          "K780807",
          "K790944",
          "K791290",
          "K992199"
        ],
        "device_name": "System, Analysis, Electrophoretic Hemoglobin",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.7440",
        "device_class": "2",
        "registration_number": [
          "1618982",
          "8023024"
        ],
        "fei_number": [
          "6387",
          "1618982"
        ]
      }
    }
  ]
}