{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Frederick",
      "address_1": "7335 Executive Way",
      "reason_for_recall": "Extended Expiration Date prior to clearance",
      "address_2": "",
      "product_quantity": "66 units",
      "code_info": "Lot Codes:  S119_2174741  S119_2161574  P119_2149301  N119_2078113  S218_2069394  V118_1991153  T118_1990945  S217_2008383  S118_1988602  P118_1996941  S117_1988305    UDI: (01)10190302006095",
      "center_classification_date": "20200414",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "MD",
      "product_description": "Oncomine Dx Target Test DNA Control-IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens, Catalog Number: A32442.",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Life Technologies Corporation",
      "recall_number": "Z-1704-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "85203",
      "termination_date": "20210326",
      "more_code_info": "",
      "recall_initiation_date": "20200316",
      "postal_code": "21704-8354",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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