{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26695",
      "product_res_number": "Z-0741-03",
      "event_date_initiated": "2003-03-18",
      "event_date_posted": "2003-04-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-11-20",
      "res_event_number": "25903",
      "k_numbers": [
        "K991513"
      ],
      "product_description": "Easypump LT 60-24\nEasypump Infusion Pump (60 ml x 2 ml/hr)",
      "code_info": "Lot numbers 04434366/2A2469 and 04434367/2A2470.",
      "firm_fei_number": "3011270181",
      "recalling_firm": "I-Flow Corporation",
      "address_1": "20202 Windrow Dr",
      "city": "Lake Forest",
      "state": "CA",
      "postal_code": "92630",
      "reason_for_recall": "Overinfusion due to misassembly.",
      "root_cause_description": "Other",
      "action": "Recall letter was sent to sole distributor, B Braun FRance by email on 3/18/2003. Return of stock and subrecall was requested. Consignee has acknowledged implementing subrecall.",
      "product_quantity": "2638 units",
      "distribution_pattern": "Only in France to distributor B. Braun Medical, France",
      "openfda": {}
    }
  ]
}