Shiley 8FENJ-SRecalls & reported problems
Covidien LP · Tracheostomy Tube Evac with Inner Cannula Fenestrated · Class 2
All models of Shiley (387)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521081601), received between Nov 7, 2019 and Jun 24, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Crack” (1 report).
23 other recalls cover devices cleared under the same FDA submission (K962173); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Crack1
- Gas/Air Leak1
- Use of Device Problem1
Patient problems
- Extubate1
- Unintended Extubation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 24, 2022Crack; Gas/Air Leak; Crack; Gas/Air Leak
ACCORDING TO THE REPORTER, THAT NIGHT AFTER THE TRACH WAS ATTACHED TO THE PATIENT LEAKS WERE FOUND AND WAS REPLACED. UPON CHECKING THEY FOUND A CRACK IN THE UPPER PART OF THE CUFF. THERE WAS NO PATIENT HARM. IT WAS UNKNOWN IF THE CUFF WAS TESTED PRIOR USING.
Patient problems: Unintended Extubation
MAUDE report 14804251 ↗InjuryNov 7, 2019Use of Device Problem; Use of Device Problem
ACCORDING TO THE REPORTER, THE DEVICE'S CUFF COULD NOT ENTER AN AIR INSIDE. THE PATIENT HAD A REPLACEMENT OF THE TUBE.
Patient problems: Extubate
MAUDE report 9293370 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K962173. One submission often covers many models, so check the product and lot details in each record.
- Z-2174-2012 · Jul 18, 2012 · TerminatedShiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes, model numbers (Worldwide) 8LPC, 8FEN; (Outside U.S.) 8FENJ, 8FENJ-S, 8LPC-S, 8FEN-S. Product Usage: The product
- Z-1463-2010 · Apr 13, 2010 · TerminatedShiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube, 6 DCT, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended f
- Z-1462-2010 · Apr 13, 2010 · TerminatedShiley Disposable Cannula Low Pressure Cuffed Tracheostomy Tube, 4 DCT, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended f
- Z-1479-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube, 6 LPC, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypass of upper
- Z-1473-2010 · Apr 13, 2010 · TerminatedShiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube, 10 DFEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, C
- Z-1481-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube, 10 LPC, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypass of upper
- Z-1491-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube with Evacuation Line, 10 LPC-S, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Inten
- Z-1488-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube with Evacuation Line, 4 LPC-S, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intend
- Z-1478-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube, 4 LPC, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypass of upper
- Z-1468-2010 · Apr 13, 2010 · TerminatedShiley Fenestrated Low Pressure Cuffed Tracheostomy Tube, 8 FEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypa
- Z-1469-2010 · Apr 13, 2010 · TerminatedShiley Fenestrated Low Pressure Cuffed Tracheostomy Tube, 10 FEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for byp
- Z-1470-2010 · Apr 13, 2010 · TerminatedShiley Disposable Cannula Fenestrated Low Pressure Cuffed Tracheostomy Tube, 4 DFEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA
- Z-1490-2010 · Apr 13, 2010 · TerminatedShiley Low Pressure Cuffed Tracheostomy Tube with Evacuation Line, 8 LPC-S, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intend
- Z-1476-2010 · Apr 13, 2010 · TerminatedShiley Fenestrated Low Pressure Cuffed Tracheostomy Tube with Evacuation Line, 6 FEN-S, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton,
- Z-1467-2010 · Apr 13, 2010 · TerminatedShiley Fenestrated Low Pressure Cuffed Tracheostomy Tube, 6 FEN, Assembled in Mexico, Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Intended for bypa
…and 8 more.
Other Tube tracheostomy and tube cuff devices
- Shiley 8CN85HCovidien LP · Tube tracheostomy and tube cuff1 recall2 deaths354 reports
- Shiley 6CN75HCovidien LP · Tube tracheostomy and tube cuff1 recall3 deaths240 reports
- Shiley 7CN80RCovidien LP · Tube tracheostomy and tube cuff2 recalls148 reports
- Bivona 67PFSS35Icu Medical, Inc. · Tube tracheostomy and tube cuff1 recall166 reports
- Bivona 670180Icu Medical, Inc. · Tube tracheostomy and tube cuff1 recall140 reports
- Bivona 670170Icu Medical, Inc. · Tube tracheostomy and tube cuff1 recall10 deaths132 reports
- Shiley 6CN75RCovidien LP · Tube tracheostomy and tube cuff1 recall1 death121 reports
- Bivona 67PFSS40Icu Medical, Inc. · Tube tracheostomy and tube cuff1 recall115 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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