Devices › Tube tracheostomy and tube cuff
Device brand name · Tracheostomy tube
Shiley Disposable Cannula Low Pressure: medical device reports filed with FDA
522 reports name it, 2008–2011. Manufacturer given most often on reports: Covidien/Formerly Tyco Healthcare. Product code JOH.
- 522
- device reports naming the brand
- 0% of all MAUDE reports · about 29 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 4%
- classified as malfunction
- 63.9% across the product code
- 0.8%
- classified as death, as reported
- 4 reports · not verified by FDA
522 medical device reports received by FDA name the brand "Shiley Disposable Cannula Low Pressure" (tracheostomy tube); the manufacturer given most often on reports is Covidien/Formerly Tyco Healthcare; received from June 2008 to October 2011. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, and none in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (95.2%), malfunction (4%) and death (0.8%); across all tube tracheostomy and tube cuff reports (product code JOH) death is recorded in 1.1% and malfunction in 63.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are air leak (51.1%), inflation problem (24.1%) and device operates differently than expected (11.1%). The patient problems coded most often are extubate, low oxygen saturation and hemorrhage/blood loss/bleeding. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
No report naming Shiley Disposable Cannula Low Pressure was received in the five years to August 2026; the latest was received in October 2011.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 15,022 reports carrying product code JOH. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Air leak | 267 | 51.1% | 11.4% |
| Inflation problem | 126 | 24.1% | 12.4% |
| Device operates differently than expectedthe device behaved unexpectedly | 58 | 11.1% | 1.5% |
| Nonstandard device | 32 | 6.1% | 0.6% |
| Deflation problem | 30 | 5.7% | 1.6% |
| Hole in material | 28 | 5.4% | 1% |
| Breakthe device broke | 25 | 4.8% | 5.1% |
| Material separation | 18 | 3.4% | 1.7% |
| Leak/splashthe device leaked | 13 | 2.5% | 7.9% |
| Difficult to insertthe device was hard to insert | 9 | 1.7% | 0.7% |
| Detachment of device component | 7 | 1.3% | 1.5% |
| Crackthe device cracked | 6 | 1.1% | 1.9% |
| Difficult to removethe device was hard to remove | 6 | 1.1% | 0.6% |
| Device dislodged or dislocated | 5 | 1% | 0.5% |
| Insufficient device problem information | 4 | 0.8% | 0.9% |
| Contamination | 3 | 0.6% | 0.4% |
| Device inoperablethe device could not be used | 3 | 0.6% | 0.1% |
| Disconnection | 3 | 0.6% | 2.4% |
| Burst container or vessel | 2 | 0.4% | 0.4% |
| Inadequacy of device shape and/or size | 2 | 0.4% | 1.2% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Extubate | 423 | 81% |
| Low oxygen saturation | 8 | 1.5% |
| Hemorrhage/blood loss/bleeding | 4 | 0.8% |
| Respiratory distressdifficulty breathing | 4 | 0.8% |
| Deaththe patient died; cause not stated by this term | 3 | 0.6% |
| Disability | 3 | 0.6% |
| Injurya physical injury | 3 | 0.6% |
| Cardiac arrestthe heart stopped | 2 | 0.4% |
| Dyspneashortness of breath | 2 | 0.4% |
| Painpain, site not specified | 2 | 0.4% |
| Pneumothoraxa collapsed lung | 2 | 0.4% |
| Airway obstruction | 1 | 0.2% |
| Anoxia | 1 | 0.2% |
| Bradycardiaslow heart rate | 1 | 0.2% |
| Brain injury | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Shiley Disposable Cannula Low Pressure | Product code JOH | All MAUDE reports |
|---|---|---|---|
| Reports | 522 | 15,022 | 26,136,888 |
| Share of that pool | — | 3.5% | 0% |
| Classified as death, per 1,000 reports | 8 | 11 | 9 |
| Classified as injury | 95.2% | 34.6% | 36.2% |
| Classified as malfunction | 4% | 63.9% | 62.3% |
| Filed by the manufacturer | 100% | 95.5% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code JOH
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Shiley | 12,236 | 1,513 | 1.1% |
| Bivona | 768 | 11 | 1% |
| Shiley Low Pressure Cuffed | 499 | 0 | 0.4% |
| Bivona Customized Tracheostomy Tubes | 200 | 24 | 1% |
| Bivona Flextend Pediatric and Neonatal Trach Tube | 180 | 44 | 0% |
| Bivona Tracheostomy Tube Neonatal/Pediatric | 232 | 7 | 0.9% |
| Shiley Fenestrated Low Pressure Cuffed | 198 | 0 | 0% |
| Portex | 970 | 8 | 0.6% |
| Portex Blue Line Ultra Tracheostomy Tube | 287 | 30 | 0% |
| Mallinckrodt | 3,105 | 1 | 1.2% |
| Portex Endotracheal Tube | 281 | 25 | 0% |
| Kangaroo Joey Pump W/Pole Clmp | 571 | 0 | 0.4% |
| Scd 700 Compression System-Us | 169 | 0 | 0% |
| Flextend | 6,836 | 203 | 0.7% |
| Level 1 Hotline Low Flow System Hl-90 | 170 | 0 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Shiley Disposable Cannula Low Pressure reports
How many FDA reports name Shiley Disposable Cannula Low Pressure?
522 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
injury (95.2%), malfunction (4%) and death (0.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
air leak (51.1%), inflation problem (24.1%), device operates differently than expected (11.1%), nonstandard device (6.1%) and deflation problem (5.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Shiley Disposable Cannula Low Pressure was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.