{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Frederick",
      "address_1": "7335 Executive Way",
      "reason_for_recall": "Extended Expiration Date prior to clearance",
      "address_2": "",
      "product_quantity": "35 units",
      "code_info": "Lot Codes:  S119_2174743  S119_2188760  S119_2165333  P119_2149298  S217_04001  1705002    UDI: (01)10190302015103",
      "center_classification_date": "20200414",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "MD",
      "product_description": "Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of DNA and RNA isolated from non-small cell lung cancer (NSCLC) tumor specimens, Catalog Number: A32441",
      "report_date": "20200422",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Life Technologies Corporation",
      "recall_number": "Z-1706-2020",
      "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"
    }
  ]
}