Catheters, suction, tracheobronchial: medical device reports filed with FDA

3,474 reports carry this product code, 1992–2026; 14 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "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."

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.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

3,474
reports with this product code: 0% of all MAUDE reports; 126
reports, 12 months to August 2026: 204 in the 12 months before; 84.9%
classified as malfunction: 62.3% across all reports; 1.2%
classified as death, as reported: 0.9% across all reports

Product code BSY is FDA's classification for "Catheters, suction, tracheobronchial" (anesthesiology panel), a class 1 device. 3,474 medical device reports carry this product code, 0% of the MAUDE database, from April 1992 to August 2026.

126 reports arrived in the 12 months to August 2026, down 38% from 204 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 malfunction (84.9%), injury (10.1%) and other (2.8%). 14 brand names with a page on this site carry this code; the brands table is 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."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Turbo-Cleaning Closed Suction System For Adults 14 F Dse	177	0	0.6%	98.9%
Dar	111	90	0.3%	92%
Argyle	8	60	1%	82.4%
Avanos	7	38	1.2%	91.2%
Medline	5	26,184	0.1%	97.9%
Cathera	3	0	7.3%	66.1%
Kendall	3	23	2.3%	61.5%
Portex	2	8	0.6%	80.6%
AirLife	1	37	2.6%	61.3%
Cardinal Health	1	185	0.2%	89.8%
Halyard	1	11	1.3%	94.9%
Rist	1	53	3%	47%
Securements	1	0	0%	100%
Tbd	1	8	0.6%	72.7%

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."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Halyard Health	1,099	31.6%
Avanos Medical	1,058	30.5%
Kimberly-Clark	46	1.3%
Carefusion	26	0.7%
Medline Industries	25	0.7%
Unomedical S R O	18	0.5%
Unomedical Sdn Bhd	13	0.4%
Convatec	10	0.3%
Vyaire Medical	9	0.3%
Smiths Healthcare Manufacturing De C V	5	0.1%
Smiths Medical International	4	0.1%
Mallinckrodt Medical	3	0.1%
Smiths Medical Asd	3	0.1%
Allegiance Healthcare	1	0%
C R Bard	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death1.2%42

Injury10.1%352

Malfunction84.9%2,950

Other2.8%98

Not given0.9%32

Who filed

Manufacturer report90.6%3,147

Voluntary report3.6%126

User facility report0%0

Distributor report0.4%13

Not given5.4%188

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Disconnection	857	24.7%
Breakthe device broke	399	11.5%
Device operates differently than expectedthe device behaved unexpectedly	306	8.8%
Suction problem	192	5.5%
Gas/air leak	164	4.7%
Suction failure	158	4.5%
Nonstandard device	120	3.5%
Detachment of device component	117	3.4%
Material separation	93	2.7%
Material integrity problema problem with the device material	91	2.6%
Air leak	90	2.6%
Leak/splashthe device leaked	85	2.4%
Detachment of device or device componentpart of the device came off	59	1.7%
Sticking	58	1.7%
Material split, cut or torn	48	1.4%
Fitting problem	43	1.2%
Crackthe device cracked	33	0.9%
Difficult to removethe device was hard to remove	33	0.9%
Physical resistance/sticking	33	0.9%
Loose or intermittent connection	31	0.9%

Questions about catheters, suction, tracheobronchial reports

What is product code BSY?

FDA's classification code for "Catheters, suction, tracheobronchial", class 1, reviewed by the anesthesiology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

3,474 reports through August 2026, 126 of them in the latest 12 months.

Which brands appear most often?

Turbo-Cleaning Closed Suction System For Adults 14 F Dse (177), Dar (111), Argyle (8), Avanos (7) and Medline (5). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

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." Brands differ in how many are in use, how long they have been sold and how reports are collected.

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. 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.