Devices › Set, administration, intravascular
Device brand name · Iv tubing
Administration Set: medical device reports filed with FDA
419 reports name it, 1996–2025. Manufacturer given most often on reports: Alaris Medical Systems. Product code FPA.
- 419
- device reports naming the brand
- 0% of all MAUDE reports · about 14 a year
- 2
- reports, 12 months to August 2026
- 34 in the 12 months before
- 86.9%
- classified as malfunction
- 79.3% across the product code
- 1.4%
- classified as death, as reported
- 6 reports · not verified by FDA
419 medical device reports received by FDA name the brand "Administration Set" (iv tubing); the manufacturer given most often on reports is Alaris Medical Systems; received from August 1996 to November 2025. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
2 reports arrived in the 12 months to August 2026, down 94% from 34 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 (86.9%), injury (11.2%) and death (1.4%); across all set, administration, intravascular reports (product code FPA) death is recorded in 0.2% and malfunction in 79.3%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are air leak (21.5%), hole in material (10%) and fluid/blood leak (9.5%). The patient problems coded most often are treatment with medication(s), overmedicated and therapy/non-surgical treatment, additional. 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
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 349,387 reports carrying product code FPA. 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 | 90 | 21.5% | 0.4% |
| Hole in material | 42 | 10% | 0.3% |
| Fluid/blood leak | 40 | 9.5% | 13.5% |
| Excess flow or over-infusion | 29 | 6.9% | 0.4% |
| Leak/splashthe device leaked | 24 | 5.7% | 11.2% |
| Material separation | 24 | 5.7% | 1.8% |
| Alarm, audible | 18 | 4.3% | 0.1% |
| Component missing | 18 | 4.3% | 0.2% |
| Misassembled | 18 | 4.3% | 0.1% |
| Occlusion within devicethe device blocked | 16 | 3.8% | 0.6% |
| Replace | 12 | 2.9% | 0.8% |
| Reflux within device | 11 | 2.6% | 0.3% |
| Failure to infuse | 10 | 2.4% | 0.3% |
| Air/gas in device | 8 | 1.9% | 0.9% |
| Detachment of device component | 8 | 1.9% | 0.6% |
| Device alarm system | 8 | 1.9% | 1.5% |
| Foreign material | 7 | 1.7% | 0.1% |
| Bubble(s) | 6 | 1.4% | 0.1% |
| Crackthe device cracked | 6 | 1.4% | 1.5% |
| Malfunction | 6 | 1.4% | 0% |
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 |
|---|---|---|
| Treatment with medication(s) | 11 | 2.6% |
| Overmedicated | 8 | 1.9% |
| Therapy/non-surgical treatment, additional | 7 | 1.7% |
| Deaththe patient died; cause not stated by this term | 6 | 1.4% |
| Retrograde flow | 5 | 1.2% |
| Air embolism | 3 | 0.7% |
| Blood glucose, low | 3 | 0.7% |
| Blood pressure, decreased | 3 | 0.7% |
| Missed dose | 3 | 0.7% |
| Other (for use when an appropriate patient code cannot be identified) | 3 | 0.7% |
| Therapy/non-surgical treatment, aborted/stopped | 3 | 0.7% |
| Therapy/non-surgical treatment/delayed/prolonged | 3 | 0.7% |
| Bleeding | 2 | 0.5% |
| Blood pressure, high | 2 | 0.5% |
| Bradycardiaslow heart rate | 2 | 0.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Administration Set | Product code FPA | All MAUDE reports |
|---|---|---|---|
| Reports | 419 | 349,387 | 26,136,888 |
| Share of that pool | — | 0.1% | 0% |
| Classified as death, per 1,000 reports | 14 | 2 | 9 |
| Classified as injury | 11.2% | 20% | 36.2% |
| Classified as malfunction | 86.9% | 79.3% | 62.3% |
| Filed by the manufacturer | 99.3% | 96.3% | 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 FPA
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Inset Guard | 47,276 | 47,222 | 0.1% |
| Inset | 26,405 | 25,656 | 0% |
| Quick Set | 23,351 | 23,028 | 0.4% |
| Autosoft Xc | 20,328 | 49 | 0% |
| Autosoft 90 | 12,143 | 15 | 0% |
| Access | 14,160 | 0 | 0% |
| Other Accessories | 10,429 | 10,425 | 1.7% |
| Alaris Pump Module Administration Set | 8,492 | 0 | 0.2% |
| Contact Detach | 6,473 | 6,157 | 0.1% |
| Inset 30 | 3,528 | 3,461 | 0% |
| Cadd | 10,811 | 9 | 0.1% |
| Minimed Quick-Set | 3,101 | 6 | 0% |
| Cleo 90 Infusion Set | 3,006 | 23 | 0% |
| Trusteel | 2,886 | 14 | 0% |
| Autosoft 30 | 2,374 | 1 | 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 Administration Set reports
How many FDA reports name Administration Set?
419 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 2 in the latest 12 months.
What kinds of events are reported?
malfunction (86.9%), injury (11.2%) and death (1.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
air leak (21.5%), hole in material (10%), fluid/blood leak (9.5%), excess flow or over-infusion (6.9%) and leak/splash (5.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.3%), voluntary reports (0.2%) and distributor reports (0.2%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Administration Set 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.