{
  "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": "LAKE FOREST",
      "address_1": "600 N FIELD DRIVE",
      "reason_for_recall": "There have been reports of distal occlusion alarms during the use of SAPPHIRE Epidural Set Yellow-Striped administration sets.",
      "address_2": "",
      "product_quantity": "31,050 units",
      "code_info": "UDI 108877870074, All codes",
      "center_classification_date": "20181217",
      "distribution_pattern": "US distribution and Internationally to Canada.",
      "state": "IL",
      "product_description": "SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch, List Number 16373-02    Sapphire Epidural Sets are indicated for the delivery of fluids from a container to a patient's epidural space. Sets are intended for use with Sapphire Infusion Systems.",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ICU Medical Inc",
      "recall_number": "Z-0619-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81615",
      "termination_date": "20201013",
      "more_code_info": "",
      "recall_initiation_date": "20181108",
      "postal_code": "60045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}