MAUDE Adverse Event Report: COVIDIEN AG JUAREZ (MMJ) Shiley; TUBE TRACHEOSTOMY AND TUBE CUFF

Model Number	7CN80A
Medical Device Problem Code	Human-Device Interface Problem (2949)
Health Effect - Clinical Codes	Hypoventilation (1916); Unintended Extubation (4564)
Date of Event	08/20/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that intra-operatively, after the patient coughed, the ventilator showed a low tidal volume, and an air leak sound was heard from the mouth and nose.Inspection of the circuit showed no abnormalities.The suction catheter could be inserted smoothly to 20 cm.The tracheostomy cuff had low tension, and after inflation it leaked repeatedly.The patient was tachypneic, but auscultation showed symmetric breath sounds in both lungs, with no obvious three-concave sign and no subcutaneous emphysema.Peripheral oxygen saturation fluctuated between 95% and 98%.Airway tube displacement and cuff leakage were considered possible.Assisted oral ventilation with a resuscitation bag was provided, and otolaryngology was asked to replace the tube with a longer one at the bedside.The patient¿s vital signs remained stable.
Additional Manufacturer Narrative
Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: Shiley
• Common Device Name: TUBE TRACHEOSTOMY AND TUBE CUFF
• Manufacturer (Section D): COVIDIEN AG JUAREZ (MMJ); 1181 hennequen ave.; juarez,chi 32575 ; MX 32575
• Manufacturer (Section G): COVIDIEN AG JUAREZ (MMJ); 1181 hennequen ave.; juarez,chi 32575 ; MX 32575
• Manufacturer Contact: mike bocchino ; 8200 coral sea st ne; mounds view, MN 55112--439 ; +1(800)646-4633
• MDR Report Key: 50532150
• Report Number: 9681384-2026-00861
• Device Sequence Number: 5951761
• Product Code: JOH
• UDI-Device Identifier: 10884521172487
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K142296
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,Company Representative
• Type of Report: Initial
• Report Date (Section B): 08/31/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 7CN80A
• Device Catalogue Number: 7CN80A
• Device Lot Number: 25D1022JZX
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/25/2026
• Initial Report FDA Received Date: 08/31/2026
• Date Device Manufactured: 04/28/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 84 YR
• Patient Sex: Male