{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Medina",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81158",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "711 Park Ave",
      "address_2": "N/A",
      "postal_code": "14103-1036",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NJ",
      "recall_number": "Z-0107-2019",
      "product_description": "SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE, 3570009",
      "product_quantity": "354 units",
      "reason_for_recall": "If an operator attempts to manually program a Basic Infusion for a drug that is not included in the Drug Library using the  Basic-Dose Mode,  the operator will receive a false  hard limit exceeded  error, preventing him or her from programming the infusion.",
      "recall_initiation_date": "20180918",
      "center_classification_date": "20181012",
      "termination_date": "20200819",
      "report_date": "20181024",
      "code_info": "UDI 00085412610900  All Serial Numbers distributed prior to 07/09/2018"
    }
  ]
}