Filter, infusion line: medical device reports filed with FDA

1,173 reports carry this product code, 1993–2026; 10 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.

1,173
reports with this product code: 0% of all MAUDE reports; 38
reports, 12 months to August 2026: 37 in the 12 months before; 88.7%
classified as malfunction: 62.3% across all reports; 0.3%
classified as death, as reported: 0.9% across all reports

Product code FPB is FDA's classification for "Filter, infusion line" (general Hospital panel), a class 2 device. 1,173 medical device reports carry this product code, 0% of the MAUDE database, from January 1993 to August 2026.

38 reports arrived in the 12 months to August 2026, close to the 37 of 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 (88.7%), injury (7.6%) and other (2.2%). 10 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
Micro-Volume Extension Set	199	0	0%	97.4%
Alaris Extension Set	77	0	0%	91.3%
Smartsite Extension Set	38	0	0.3%	93.7%
Medex	14	8	0%	81.7%
Interlink	11	49	0%	92.1%
Smallbore Extension Set	10	0	0%	91.2%
Extension Set	5	66	1.3%	56.6%
Administration Set	4	2	1.4%	86.9%
B Braun	2	12	3%	77.8%
Medfusion	1	0	0.1%	99.1%

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	158	13.5%
Carefusion	115	9.8%
Baxter Healthcare - Aibonito	56	4.8%
Hospira	42	3.6%
Smiths Healthcare Manufacturing De C V	24	2%
Baxter Healthcare - Cleveland	22	1.9%
Smiths Medical Asd	18	1.5%
Baxter International	6	0.5%
Hospira Costa Rica	6	0.5%
B Braun Medical	4	0.3%
Abbott Laboratories	3	0.3%
B Braun Melsungen	2	0.2%
Davol	2	0.2%
Icu Medical	2	0.2%
Abbott	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

Death0.3%3

Injury7.6%89

Malfunction88.7%1,040

Other2.2%26

Not given1.3%15

Who filed

Manufacturer report83.4%978

Voluntary report9.5%111

User facility report0%0

Distributor report0.2%2

Not given7%82

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

Device problems coded

Device problem (FDA code)	Reports	Share
Fluid/blood leak	531	45.3%
Leak/splashthe device leaked	198	16.9%
Crackthe device cracked	131	11.2%
Filter leak(s)	87	7.4%
Air leak	55	4.7%
Disconnection	54	4.6%
Material separation	36	3.1%
Breakthe device broke	32	2.7%
No flow	23	2%
Occlusion within devicethe device blocked	16	1.4%
Replace	15	1.3%
Hole in material	14	1.2%
Device contamination with chemical or other material	13	1.1%
Material discolored	12	1%
Obstruction of flow	11	0.9%
Backflow	10	0.9%
Failure to deliverthe device did not deliver the dose or item	10	0.9%
Material puncture/hole	10	0.9%
Complete blockage	9	0.8%
Device displays incorrect message	9	0.8%

Questions about filter, infusion line reports

What is product code FPB?

FDA's classification code for "Filter, infusion line", class 2, reviewed by the general Hospital panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,173 reports through August 2026, 38 of them in the latest 12 months.

Which brands appear most often?

Micro-Volume Extension Set (199), Alaris Extension Set (77), Smartsite Extension Set (38), Medex (14) and Interlink (11). 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.