{
  "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": "Englewood",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72331",
      "recalling_firm": "WalkMed Infusion, LLC",
      "address_1": "6555 S Kenton St Ste 304",
      "address_2": "N/A",
      "postal_code": "80111-6838",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of AL, CA, CO, DE, FL, GA, IL, MA, MD, MI, MN, MS, NC, NJ, NM, NV, NY, OH, PA, TN, TX, and WA.",
      "recall_number": "Z-0242-2016",
      "product_description": "Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump).  Used to pump fluids into a patient in a controlled manner.",
      "product_quantity": "4695 units",
      "reason_for_recall": "The device might fail to detect air in line while infusing the medication Venofer.  This may occur when a drop of Venofer gets stuck in the tubing adjacent to the bubble detector and the Total Volume Limit is programmed higher than the actual bag volume.",
      "recall_initiation_date": "20151001",
      "center_classification_date": "20151106",
      "termination_date": "20160712",
      "report_date": "20151118",
      "code_info": "Model numbers 300000, 400000"
    }
  ]
}