{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Turku",
      "state": "N/A",
      "country": "Finland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72013",
      "recalling_firm": "Perkin Elmer Life Sciences Inc",
      "address_1": "Laitun 4  Mustionkatu 6",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to FL, GA,  and NV; and Canada",
      "recall_number": "Z-0166-2016",
      "product_description": "Perkin Elmer Specimen Gate, Screening Center.  Data management of neonatal screening test results and demographics by qualified laboratory personnel in newborn screening programs.",
      "product_quantity": "6 units",
      "reason_for_recall": "It would be possible for an abnormal analytical test result value from an affected newborn to be reported with a default result interpretation of normal. The analytical test result value would be correct but the interpretation of the test result value would be incorrect.",
      "recall_initiation_date": "20150824",
      "center_classification_date": "20151026",
      "termination_date": "20210121",
      "report_date": "20151104",
      "code_info": "Software Version 1.6"
    }
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}