Cabinet, table and tray, anesthesia: medical device reports filed with FDA

103,373 reports carry this product code, 1992–2026; 22 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.

103,373
reports with this product code: 0.4% of all MAUDE reports; 64,695
reports, 12 months to August 2026: 37,080 in the 12 months before; 99.9%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code BRY is FDA's classification for "Cabinet, table and tray, anesthesia" (anesthesiology panel), a class 1 device. 103,373 medical device reports carry this product code, 0.4% of the MAUDE database, from May 1992 to August 2026.

64,695 reports arrived in the 12 months to August 2026, up 74% from 37,080 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 (99.9%), injury (0.1%) and other (0.1%). 22 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
BD Pyxis MedStation ES	49,097	33,499	0%	99.9%
BD Pyxis MedStation ES Auxiliary	14,382	9,862	0%	99.9%
BD Pyxis Anesthesia Station ES	6,844	4,515	0%	99.8%
Pyxis Medstation Es System	6,114	0	0%	100%
BD Pyxis MedStation ES Auxiliary Tower	5,488	3,659	0%	99.9%
BD Pyxis ES Server	5,487	4,442	0%	99.9%
BD Pyxis MedBank Tower	4,510	3,170	0%	99.9%
BD Pyxis ES Refrigerator	1,258	949	0%	100%
BD Pyxis MedBank Mini	1,067	768	0%	100%
Pyxis Medstation System	977	0	0%	100%
BD Pyxis MedStation ES Tower	905	634	0%	100%
BD Pyxis Medflex 1000	890	676	0%	99.9%
Pyxis Anesthesia System Pas	797	0	0%	98.5%
BD Pyxis MedStation 4000	483	284	0%	100%
BD Pyxis MedBank Tower Aux	472	300	0%	100%
Bd Pyxis Medstation Es System	427	5	0.2%	98.4%
Bd Pyxis Medbank	314	150	0%	100%
Pyxis Medbank System	274	0	0%	100%
Bd Pyxis Anesthesia System Es	191	2	0%	99.5%
BD Pyxis Medflex 2000	174	120	0%	100%
Bd Pyxis Medstation Es Main	169	0	0%	98.8%
Bd Pyxis Medbank Twr Mn 12hh-1fh	151	151	0%	100%

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
Carefusion 303	102,655	99.3%
Carefusion	259	0.3%
Carefusion Sd	1	0%
Keymed Medical And Industrial Equipment	1	0%
Sistemas Medicos Alaris De C V	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

Death0%12

Injury0.1%78

Malfunction99.9%103,221

Other0.1%56

Not given0%6

Who filed

Manufacturer report99.9%103,305

Voluntary report0%36

User facility report0%0

Distributor report0%1

Not given0%31

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

Device problems coded

Device problem (FDA code)	Reports	Share
Mechanical problema mechanical problem	23,140	22.4%
Computer software problema software problem	11,389	11%
Application program problem	10,464	10.1%
Loose or intermittent connection	9,687	9.4%
Circuit failure	8,392	8.1%
Electrical /electronic property probleman electrical or electronic problem	7,902	7.6%
Breakthe device broke	6,608	6.4%
Activation failure	5,863	5.7%
Failure to eject	5,304	5.1%
Labelling, instructions for use or training problem	4,858	4.7%
Communication or transmission problemthe device could not communicate or transmit	4,221	4.1%
Application network problem	2,996	2.9%
Installation-related problem	2,920	2.8%
Application program freezes or fails to launch	2,681	2.6%
Contamination	2,650	2.6%
Mechanical jam	2,526	2.4%
Component missing	2,230	2.2%
Failure to align	1,183	1.1%
Thermal decomposition of device	983	1%
Data problem	706	0.7%

Questions about cabinet, table and tray, anesthesia reports

What is product code BRY?

FDA's classification code for "Cabinet, table and tray, anesthesia", class 1, reviewed by the anesthesiology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

103,373 reports through August 2026, 64,695 of them in the latest 12 months.

Which brands appear most often?

BD Pyxis MedStation ES (49,097), BD Pyxis MedStation ES Auxiliary (14,382), BD Pyxis Anesthesia Station ES (6,844), Pyxis Medstation Es System (6,114) and BD Pyxis MedStation ES Auxiliary Tower (5,488). 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.