{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Morrisville",
      "address_1": "5151 McCrimmon Pkwy Ste 250",
      "reason_for_recall": "Labeling: The labeled storage temperature is not consistent with the temperature conditions tested for the entire four year shelf life duration.",
      "address_2": "",
      "product_quantity": "94,095 units.",
      "code_info": "Model number LFD-1000 and LFD-1100, All lots",
      "center_classification_date": "20170322",
      "distribution_pattern": "US (nationwide)",
      "state": "NC",
      "product_description": "LipiFlow Thermal Pulsation System/LipiFlow, System Activator (Disposable), Rx Only, Sterile",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tearscience, Inc",
      "recall_number": "Z-1535-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76365",
      "termination_date": "20171127",
      "more_code_info": "",
      "recall_initiation_date": "20170130",
      "postal_code": "27560-5427",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}