{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "167106",
      "product_res_number": "Z-0113-2019",
      "event_date_initiated": "2018-07-24",
      "event_date_created": "2018-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-05-26",
      "res_event_number": "80954",
      "product_code": "JHS",
      "k_numbers": [
        "K962126"
      ],
      "product_description": "ADVIA Centaur CKMB Calibrator, Cat No. 09318028\n\nProduct Usage:\nFor in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.",
      "code_info": "SMN 10311570  Lot # Expiry UDI # 57834A64 2018-Dec-11 (01)00630414124803(10)57834A64(17)20181211 57835A64 2018-Dec-11 (01)00630414124803(10)57835A64(17)20181211 72519A64 2018-Dec-11 (01)00630414124803(10)72519A64(17)20181211 98115A64 2018-Dec-11 (01)00630414124803(10)98115A64(17)20181211",
      "firm_fei_number": "1219913",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc",
      "address_1": "333 Coney St",
      "city": "East Walpole",
      "state": "MA",
      "postal_code": "02032-1516",
      "additional_info_contact": "508-668-5000",
      "reason_for_recall": "A potential bias was identified with certain kits compared to the internal standards.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "On July 24, 2018 Siemens Healthineers issued Urgent Medical Device Recall notices to U.S. customers and Urgent Field Safety Notices to OUS customers.  \n\nThe following are Actions to be Taken by the Customer:\n\nCustomers using ADVIA Centaur CKMB Calibrator Lots ending in 64:\n- Review the notice with your Medical Director.\n- Review your inventory of these products and immediately order replacement ADVIA Centaur CKMB Calibrator kit lots ending in 68 by completing the Field Correction Effectiveness Check Form attached to the letter.\n- You may continue use of ADVIA Centaur CKMB Calibrator kit lots until\nreplacement product is received in your laboratory. \n- Upon receipt of replacement product in your laboratory, discontinue use of and discard the ADVIA Centaur CKMB Calibrator kit lots listed in Table 1 of the letter.\n- ADVIA Centaur CKMB Calibrator kit lots ending in 63 may continue to be used until the assigned expiration date.  \n- Refer to the Additional Information section for expected patient sample bias when transitioning to ADVIA Centaur CKMB Calibrator kit lots ending in 68.\n\nCustomers using ADVIA Centaur Master Curve Material:\n- Discontinue use of and discard the ADVIA Centaur MCM lots in Table 1.\n- Review your inventory of these products and order replacement ADVIA Centaur CKMB Master Curve Material by completing the Field Correction Effectiveness Check Form attached to the letter.\n- Utilize ADVIA Centaur CKMB MCM Lot 13384 and future lots.\n- Complete and return the Field Correction Effectiveness Check Form attached to the letter within 30 days.\n\nCustomers using Atellica IM CKMB Calibrator Lots ending in 66:\n- Review your inventory of these products and immediately order replacement Atellica IM CKMB Calibrator kit lots ending in 69 by completing the Field Correction Effectiveness Check Form attached to the letter.\n- You may continue use of Atellica IM CKMB Calibrator kit lots in Table 1 until replacement product is received in your laboratory",
      "product_quantity": "1870 kits",
      "distribution_pattern": "US Nationwide Distribution",
      "openfda": {
        "k_number": [
          "K160570",
          "K820722",
          "K790015",
          "K810997",
          "K801668",
          "K800028",
          "K082226",
          "K872029",
          "K062128",
          "K861387",
          "K790088",
          "K945083",
          "K802521",
          "K781690",
          "K823211",
          "K803169",
          "K792023",
          "K780504",
          "K952250",
          "K981495",
          "K790343",
          "K854708",
          "K990434",
          "K781432",
          "K855188",
          "K900806",
          "K883223",
          "K790917",
          "K843007",
          "K102706",
          "K941584",
          "K790918",
          "K790916",
          "K903025",
          "K962126",
          "K813406",
          "K943024",
          "K990439"
        ],
        "registration_number": [
          "1219913",
          "9681753",
          "2432235",
          "1319681",
          "1319809",
          "2517506",
          "9610529",
          "9610126",
          "3003795116",
          "2250051",
          "3006198300"
        ],
        "fei_number": [
          "1219913",
          "2432235",
          "3002806559",
          "1000136573",
          "2517506",
          "3000303338",
          "3003795116",
          "3002806560",
          "2250051",
          "1000305840",
          "3006198300"
        ],
        "device_name": "Differential Rate Kinetic Method, Cpk Or Isoenzymes",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1215",
        "device_class": "2"
      }
    }
  ]
}