{
  "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": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64826",
      "recalling_firm": "I-Flow LLC",
      "address_1": "20202 Windrow Dr",
      "address_2": "N/A",
      "postal_code": "92630-8152",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide distribution: USA including states of:  CA, CT, FL, IL, IN, KY, NY, OH, OR, TN, TX, VA and WI.",
      "recall_number": "Z-1444-2013",
      "product_description": "I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Tray, Model #TBTB1089T    The intended use of each component in the finished final trays is consistent with the intended use of the component stated in the respective 510(k) submission.",
      "product_quantity": "450 units",
      "reason_for_recall": "I-Flow initiated two voluntary product removals of the ON-Q Pain Relief System: T-Block Needle/Catheter Tray and T-Block Needle/Catheter Kit because they may have potentially malfunctioned.",
      "recall_initiation_date": "20120601",
      "center_classification_date": "20130603",
      "termination_date": "20130625",
      "report_date": "20130612",
      "code_info": "Lot # AW207202O"
    }
  ]
}