{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "96004",
      "product_res_number": "Z-0902-2011",
      "event_date_initiated": "2010-10-25",
      "event_date_posted": "2011-01-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-04-17",
      "res_event_number": "57377",
      "product_code": "LSZ",
      "pma_numbers": [
        "P850064"
      ],
      "product_description": "One Cat. Life Pulse High Frequency Ventilator, Catalog Number: 203, Manufactured by: Bunnell Incorporated Salt Lake City, Utah, Rx Only.",
      "code_info": "Model 203",
      "firm_fei_number": "3032745446",
      "recalling_firm": "Bunnell, Inc.",
      "address_1": "436 Lawndale Dr",
      "city": "Salt Lake City",
      "state": "UT",
      "postal_code": "84115-2917",
      "additional_info_contact": "Diane M. Goodman\n801-467-0800",
      "reason_for_recall": "Product software coding error may compromise patient safety.",
      "root_cause_description": "Software design",
      "action": "Customers were notified by an \"Urgent: Medical Device Recall or Correction\" letter starting 10/22/10.  The letter identified the product and described the issues.  Customers were given the option of either returning their ventilator(s) for rework or to receive installation/re-test instructions with an upgrade kit to rework themselves.  The letter states that all Life Pulse ventilators in clinical use must be upgraded and there is no charge for the software upgrade.",
      "product_quantity": "660 total",
      "distribution_pattern": "Worldwide Distribution -- USA, Australia, Canada, Czech Republic, Korea, Malaysia, Trinidad & Tobago, and Uruguay.",
      "openfda": {
        "pma_number": [
          "P890057",
          "P890034",
          "P880013",
          "P850064"
        ],
        "device_name": "Ventilator, High Frequency",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "registration_number": [
          "2021710",
          "3032745446",
          "8030673",
          "1220908",
          "1314417"
        ],
        "fei_number": [
          "2021710",
          "3032745446",
          "1220908",
          "1314417",
          "3004213967"
        ]
      }
    }
  ]
}