System, dialysate delivery, single patient: medical device reports filed with FDA

1,072 reports carry this product code, 1992–2021; 6 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.

1,072
reports with this product code: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 56.6%
classified as malfunction: 62.3% across all reports; 8.7%
classified as death, as reported: 0.9% across all reports

Product code FKP is FDA's classification for "System, dialysate delivery, single patient" (gastroenterology, Urology panel), a class 2 device. 1,072 medical device reports carry this product code, 0% of the MAUDE database, from September 1992 to July 2021.

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 malfunction (56.6%), injury (27.6%) and death (8.7%). 6 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
System 1000 Spds	385	0	3.1%	75.1%
1550 Hemodialysis Machine	224	0	10.6%	53.3%
Fresenius	4	0	6.1%	13.7%
Phoenix	4	16	5.5%	32.9%
Cobe Centrysystem 3	3	0	0.8%	83.3%
Fresenius Dialysis Delivery System	3	0	11%	60.4%

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
Baxter Healthcare	658	61.4%
Fresenius USA	19	1.8%
Baxter Healthcare - Largo	13	1.2%
Nxstage Medical	10	0.9%
Gambro Healthcare	9	0.8%
Concord Manufacturing	4	0.4%
Fresenius Medical Care North America	4	0.4%
Reynosa Manufacturing	1	0.1%
Terumo Medical	1	0.1%

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

Death8.7%93

Injury27.6%296

Malfunction56.6%607

Other6.2%66

Not given0.9%10

Who filed

Manufacturer report81.9%878

Voluntary report4.3%46

User facility report0%0

Distributor report1.9%20

Not given11.9%128

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

Device problems coded

Device problem (FDA code)	Reports	Share
Device alarm system	123	11.5%
Output, high	74	6.9%
Replace	69	6.4%
Other (for use when an appropriate device code cannot be identified)	66	6.2%
Inadequate ultra filtration	53	4.9%
Insufficient flow or under infusion	48	4.5%
Self-activation or keying	48	4.5%
Conductivity	44	4.1%
Air leak	43	4%
Output, low	43	4%
Excess flow or over-infusion	38	3.5%
Alarm, audible	36	3.4%
Leak/splashthe device leaked	33	3.1%
Loss of powerthe device lost power	31	2.9%
Underdelivery	27	2.5%
Transducer failure	22	2.1%
Device contamination with body fluid	21	2%
Device displays incorrect message	21	2%
Device issuea problem with the device	21	2%
Dislodged	20	1.9%

Questions about system, dialysate delivery, single patient reports

What is product code FKP?

FDA's classification code for "System, dialysate delivery, single patient", class 2, reviewed by the gastroenterology, Urology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,072 reports through August 2026, 0 of them in the latest 12 months.

Which brands appear most often?

System 1000 Spds (385), 1550 Hemodialysis Machine (224), Fresenius (4), Phoenix (4) and Cobe Centrysystem 3 (3). 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.