{
  "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": "131410",
      "product_res_number": "Z-0850-2015",
      "event_date_initiated": "2014-11-06",
      "event_date_posted": "2014-12-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-03-17",
      "res_event_number": "69715",
      "product_code": "PFS",
      "k_numbers": [
        "K132750"
      ],
      "product_description": "Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay  in vitro diagnostic system for use on the Illumina MiSeqDx Platform.",
      "code_info": "Instrument Serial No. M70106, M00533L, M70114. Lot No. Shipped: K103313, K103461, K103404, K103487.",
      "firm_fei_number": "3003218906",
      "recalling_firm": "Illumina Inc",
      "address_1": "5200 Illumina Way",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121",
      "additional_info_contact": "858-736-3861",
      "reason_for_recall": "Illumina has confirmed a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay on the MiSeqDx instrument.",
      "root_cause_description": "Under Investigation by firm",
      "action": "A customer notification letter dated 11/12/14 was sent to all customers who purchased the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay.  The letter confirms that there is a software limitation with MiSeq Reporter software (version 2.2.31) when using the MiSeqDx Cystic Fibrosis Clinical Sequencing Assay on the MiSeqDx instrument.  At certain genomic locations within the region sequenced by the assay, deletions cannot be reported by the software. The letter outlines the potential issues, the results of Illuminia's investigation, and the firm's next steps.  Customers' with technical questions or concerns, are instructed to contact their local support team or Illumina Technical Support at techsupport@illumina.com.  Customers with questions regarding the field action, are instructed to contact Illumina Regulatory Affairs at RA@illumina.com.\n\nCustomers will be contacted by 11/13/14 by phone and a phone script was provided that includes the procedure, talking points, actions required, and next steps.",
      "product_quantity": "19 units",
      "distribution_pattern": "US: MD, NY \nNon-US: France",
      "openfda": {
        "k_number": [
          "K132750"
        ],
        "registration_number": [
          "3003218906"
        ],
        "fei_number": [
          "3003218906"
        ],
        "device_name": "System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection",
        "medical_specialty_description": "Immunology",
        "regulation_number": "866.5900",
        "device_class": "2"
      }
    }
  ]
}