{
  "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": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "1265 Grey Fox Rd",
      "reason_for_recall": "An issue with the plunger rod seal was identified where the seal had the potential to migrate inside the pump case top during slow rate/ high back pressure infusions.",
      "address_2": "",
      "product_quantity": "6",
      "code_info": "Lot/Serial Numbers: M76369, M76370, M76373, M76374, M76375, and M76377.",
      "center_classification_date": "20130326",
      "distribution_pattern": "Distributed in the state of NH.",
      "state": "MN",
      "product_description": "Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500.    Intended for use in critical care areas for the administration of fluids requiring precisely controlled infusion rates.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smiths Medical ASD, Inc.",
      "recall_number": "Z-0996-2013",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "63621",
      "termination_date": "20130411",
      "more_code_info": "",
      "recall_initiation_date": "20100514",
      "postal_code": "55112-6929",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}