{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "5200 Illumina Way",
      "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.",
      "address_2": "",
      "product_quantity": "19 units",
      "code_info": "Instrument Serial No. M70106, M00533L, M70114.  Lot No. Shipped: K103313, K103461, K103404, K103487.",
      "center_classification_date": "20141223",
      "distribution_pattern": "US: MD, NY   Non-US: France",
      "state": "CA",
      "product_description": "Illumina MiSeqDx Cystic Fibrosis Clinical Sequencing Assay  in vitro diagnostic system for use on the Illumina MiSeqDx Platform.",
      "report_date": "20141231",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Illumina Inc",
      "recall_number": "Z-0850-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
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      "termination_date": "20150317",
      "more_code_info": "",
      "recall_initiation_date": "20141106",
      "postal_code": "92121",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}