{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Boulder",
      "address_1": "6135 Gunbarrel Ave",
      "reason_for_recall": "Graphical user interface (GUI) unresponsive to touch and Loss of primary ventilation under certain circumstances.  Covidien Respiratory and Monitoring Solutions, now a part of Medtronic, issued a field corrective action notice for two issues on all models of Puritan Bennett 980 (PB980) ventilator.",
      "address_2": "",
      "product_quantity": "1,864 units",
      "code_info": "all versions of software.",
      "center_classification_date": "20160316",
      "distribution_pattern": "Worldwide Distribution -- US, including but not limited to the territory of Puerto Rico; and Ireland, Jordan, Saudi Arabia, Bahrain, Australia, Japan, Israel, Turkey, Chile, South Africa, Costa Rica, United Arab Emirates, Qatar, Peru, Panama, Singapore, Kuwait,  Lebanon, Brazil, Mexico, Colombia, Russia, Uruguay, Slovenia, Morocco, Argentina, Egypt, and Romania.",
      "state": "CO",
      "product_description": "Puritan Bennett 980 Ventilator System, PB980 Ventilator (980xxxxxxxx).    Intended to provide continuous ventilation for pediatric and adult patients who require either invasive ventilation or non-invasive ventilation.",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Covidien LP (formerly Nellcor Puritan Bennett Inc.)",
      "recall_number": "Z-1181-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73096",
      "termination_date": "20170711",
      "more_code_info": "",
      "recall_initiation_date": "20160115",
      "postal_code": "80301-3214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}