{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Boulder",
      "address_1": "6135 Gunbarrel Ave",
      "reason_for_recall": "Covidien is conducting a voluntary field corrective action on Puritan Bennett 840 ventilator systems with certain software revisions in response to customer reports of ventilator diagnostic code XB0069 in which the device stops mechanical ventilation due to a software error.",
      "address_2": "",
      "product_quantity": "16,923 US, 39,372 OUS",
      "code_info": "Software Part number 4-070212-85, revision AB-AG",
      "center_classification_date": "20140103",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Austria, Estonia, Belgium, Spain, Italy, Poland, Bulgaria, Finland, Portugal, Switzerland, France, Lithuania, Romania, Cyprus, Great Britain, Czech Republic, Greece, Latvia, Slovenia, Germany, Hungary, Slovak Republic, Ireland, Netherlands, Turkey, Croatia, Andorra, Albania, Algeria, Bahrain, Bosnia and Herzegovina, Egypt, Georgia, Iran, Iraq, Israel, Jordan, Kenya, Kuwait, Lebanon, Libya, Macedonia, Montenegro, Morocco, Russia, Saudi Arabia, Serbia, South Africa, Syria, Sudan, Tunisia, UAE, Uganda, Puerto Rico, Mexico, Columbia, Chile, Brazil, Argentina, Uruguay, Panama, Costa Rica, Peru, China, Korea, Japan, Taiwan, Hong Kong, Malaysia, Singapore, Sri Lanka, Australia, New Zealand.",
      "state": "CO",
      "product_description": "Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG.    The intended use of the product is to provide mechanical ventilation to patients.",
      "report_date": "20140115",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Covidien",
      "recall_number": "Z-0611-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67108",
      "termination_date": "20161129",
      "more_code_info": "",
      "recall_initiation_date": "20131216",
      "postal_code": "80301-3214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}