Device brand name · Pump infusion
Alaris Pump Module: medical device reports filed with FDA
684,522 reports name it, 2009–2022. Manufacturer given most often on reports: Carefusion Sd. Product code FRN.
- 684,522
- device reports naming the brand
- 2.6% of all MAUDE reports · about 39,692 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 99.7%
- classified as malfunction
- 98.5% across the product code
- 0%
- classified as death, as reported
- 167 reports · not verified by FDA
FDA's MAUDE database holds 684,522 reports that name the brand "Alaris Pump Module" (pump infusion), received between April 2009 and December 2022; the manufacturer given most often on reports is Carefusion Sd. Spellings of one product vary from report to report.
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 (99.7%) and injury (0.2%); across all pump, infusion reports (product code FRN) death is recorded in 0.1% and malfunction in 98.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are crack (93.7%), display difficult to read (2.4%) and display or visual feedback problem (2.2%). The patient problems coded most often are no patient involvement, overdose and low blood pressure/ hypotension. 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 1,831,109 reports carrying product code FRN. 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 |
|---|---|---|---|
| Crackthe device cracked | 641,591 | 93.7% | 40.3% |
| Display difficult to read | 16,362 | 2.4% | 5% |
| Display or visual feedback problem | 15,130 | 2.2% | 1.1% |
| Excess flow or over-infusion | 3,081 | 0.5% | 1.2% |
| Device alarm system | 1,386 | 0.2% | 2.8% |
| Breakthe device broke | 1,350 | 0.2% | 8.5% |
| Electrical /electronic property probleman electrical or electronic problem | 999 | 0.1% | 0.8% |
| Insufficient flow or under infusion | 760 | 0.1% | 0.8% |
| Insufficient device problem information | 679 | 0.1% | 0.8% |
| Pumping stopped | 610 | 0.1% | 0.2% |
| Failure to read input signal | 605 | 0.1% | 3% |
| Failure to cycle | 584 | 0.1% | 0% |
| Pressure problem | 571 | 0.1% | 0.1% |
| Physical resistance/sticking | 412 | 0.1% | 1.2% |
| Corrodedthe device corroded | 405 | 0.1% | 11.6% |
| Device sensing problem | 383 | 0.1% | 3.8% |
| Device displays incorrect message | 363 | 0.1% | 9.3% |
| Infusion or flow problema problem with flow or infusion | 320 | 0% | 0.3% |
| Communication or transmission problemthe device could not communicate or transmit | 309 | 0% | 0.5% |
| Calibration problem | 306 | 0% | 0.4% |
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 |
|---|---|---|
| No patient involvement | 17,294 | 2.5% |
| Overdosea dose above the recommended amount | 399 | 0.1% |
| Low blood pressure/ hypotension | 368 | 0.1% |
| Deaththe patient died; cause not stated by this term | 152 | 0% |
| Therapeutic response, increased | 132 | 0% |
| High blood pressure/ hypertension | 111 | 0% |
| Hypoglycemialow blood sugar | 84 | 0% |
| Hyperglycemiahigh blood sugar | 68 | 0% |
| Underdoseless than the intended dose | 63 | 0% |
| Bradycardiaslow heart rate | 60 | 0% |
| Therapeutic response, decreased | 46 | 0% |
| Tachycardiafast heart rate | 43 | 0% |
| Cardiac arrestthe heart stopped | 40 | 0% |
| Infiltration into tissue | 39 | 0% |
| Venipuncture | 29 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Alaris Pump Module | Product code FRN | All MAUDE reports |
|---|---|---|---|
| Reports | 684,522 | 1,831,109 | 26,136,888 |
| Share of that pool | — | 37.4% | 2.6% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 0.2% | 1.3% | 36.2% |
| Classified as malfunction | 99.7% | 98.5% | 62.3% |
| Filed by the manufacturer | 100% | 99.1% | 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 FRN
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Alaris System | 422,501 | 33,692 | 0% |
| 8100 Alaris Pump Module | 163,620 | 0 | 0% |
| Spectrum Infusion Pump | 147,363 | 15 | 0% |
| 8015 Alaris System Pc Unit | 54,162 | 0 | 0% |
| Alaris System Pc Unit | 24,066 | 0 | 0% |
| 8110 Alaris Syringe Pump | 22,434 | 0 | 0% |
| Colleague | 21,763 | 0 | 0% |
| Reservoir 3ML MMT-332A | 19,914 | 2,008 | 0.4% |
| Reservoir 3ml | 16,407 | 0 | 0.8% |
| Flogard | 15,668 | 0 | 0% |
| Colleague Volumetric Infusion Pump | 13,678 | 0 | 0.1% |
| Colleague Pre P1 7 | 13,103 | 0 | 0% |
| CADD-Solis VIP Ambulatory Infusion Pump | 11,721 | 3,471 | 0.1% |
| Intermate | 8,261 | 47 | 0% |
| Reservoir 1 8ml | 7,952 | 0 | 0.1% |
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." 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 Alaris Pump Module reports
How many FDA reports name Alaris Pump Module?
684,522 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (99.7%) and injury (0.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
crack (93.7%), display difficult to read (2.4%), display or visual feedback problem (2.2%), excess flow or over-infusion (0.5%) and device alarm system (0.2%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%) and voluntary reports (0%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Alaris Pump Module 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.