{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "190187",
      "product_res_number": "Z-0346-2022",
      "event_date_initiated": "2021-11-04",
      "event_date_posted": "2021-12-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2024-07-09",
      "res_event_number": "88987",
      "product_code": "CBK",
      "k_numbers": [
        "K193056"
      ],
      "product_description": "Puritan Bennett 980 Series Ventilator, 980X1ENDIPC",
      "code_info": "GTIN/UDI - 10884521172302\n\nSerial Numbers:\n35B1700447\n35B1700405",
      "firm_fei_number": "1282497",
      "recalling_firm": "Covidien Llc",
      "address_1": "15 Hampshire St",
      "city": "Mansfield",
      "state": "MA",
      "postal_code": "02048-1113",
      "additional_info_contact": "Technical Service\n508-261-8000",
      "reason_for_recall": "Manufacturing assembly error where a capacitor within the ventilator was assembled incorrectly, which may cause the device to become inoperable during use.",
      "root_cause_description": "Reprocessing Controls",
      "action": "On November 4, 2021, the firm began to notify customers through Urgent Medical Device Correction letters. Customers were informed of the device defect that may lead to the ventilator becoming inoperable during use.\n\nActions you should take\n\n Immediately discontinue use of the affected ventilators. Remove the affected ventilators from clinical service and quarantine the affected ventilators until such time that a Medtronic Technical Service Engineer inspects and replaces the affected printed circuit board assemblies.\n\n Notify all personnel in all care environments in which the affected PB980 series ventilators are used about this medical device correction.\n\n If your facility has distributed affected PB980 series ventilators to other persons or facilities, please promptly forward a copy of this letter to those recipients.\n\n Complete the attached form and return it as directed to confirm your receipt and understanding of this information.\n\n If you are aware of any incidents related to this issue, please contact our Technical Support Department immediately at 1-800-255-6774, option 4, and then option 1 to provide information regarding those events so regulatory reporting obligations can be fulfilled.\n\n Work with the Medtronic Technical Support Department if you require assistance finding alternative ventilation devices.\n\nBeginning November 5, 2021, Medtronic Technical Service will contact all affected customers to schedule a service appointment for all potentially affected ventilators.\n\nIf you have any questions regarding this communication, please contact your Medtronic representative or Technical Service at 1-800-255-6774.",
      "product_quantity": "278 total",
      "distribution_pattern": "Worldwide distribution - US Nationwide.",
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