{
  "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": "2026-08-13",
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      "cfres_id": "30770",
      "product_res_number": "Z-0300-04",
      "event_date_initiated": "2003-11-07",
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      "recall_status": "Terminated",
      "event_date_terminated": "2016-02-01",
      "res_event_number": "27937",
      "product_code": "MNT",
      "product_description": "MVP-10 Pediatric/ Neonatal Volume Ventilator",
      "code_info": "S/N: 3023031, 3025031, 0957951",
      "firm_fei_number": "3003952420",
      "recalling_firm": "Bio-Med Devices, Inc.",
      "address_1": "1445 Boston Post Rd",
      "city": "Guilford",
      "state": "CT",
      "postal_code": "06437-4338",
      "additional_info_contact": "Ken Close\n203-458-0202 Ext. 17",
      "reason_for_recall": "Two way relief valve may fail to activate at the low negative pressure of  -3cm H2O.",
      "root_cause_description": "Other",
      "action": "Bio Med Devices notified accounts by telephone on 11/7/03, to return the device for replacement and correction.",
      "product_quantity": "3 units",
      "distribution_pattern": "ID, PA, TX",
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