Device brand name · Pump infusion
Intermate: medical device reports filed with FDA
8,261 reports name it, 2010–2026. Manufacturer given most often on reports: Baxter Healthcare - Irvine. Product code FRN.
- 8,261
- device reports naming the brand
- 0% of all MAUDE reports · about 503 a year
- 47
- reports, 12 months to August 2026
- 46 in the 12 months before
- 99.9%
- classified as malfunction
- 98.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
8,261 medical device reports received by FDA name the brand "Intermate" (pump infusion); the manufacturer given most often on reports is Baxter Healthcare - Irvine; received from February 2010 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
47 reports arrived in the 12 months to August 2026, close to the 46 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 (99.9%) and injury (0.1%); 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 device contamination with chemical or other material (55.7%), material rupture (12.5%) and component missing (6.5%). The patient problems coded most often are no patient involvement, underdose and injury. 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 |
|---|---|---|---|
| Device contamination with chemical or other material | 4,604 | 55.7% | 0.3% |
| Material rupture | 1,034 | 12.5% | 0.1% |
| Component missing | 535 | 6.5% | 0.1% |
| Fluid/blood leak | 453 | 5.5% | 0.6% |
| Breakthe device broke | 406 | 4.9% | 8.5% |
| Filling problem | 179 | 2.2% | 0.2% |
| Leak/splashthe device leaked | 156 | 1.9% | 0.3% |
| Crackthe device cracked | 144 | 1.7% | 40.3% |
| No flow | 120 | 1.5% | 0.1% |
| Detachment of device component | 118 | 1.4% | 0% |
| Disconnection | 99 | 1.2% | 0% |
| Device operates differently than expectedthe device behaved unexpectedly | 93 | 1.1% | 0.9% |
| Material separation | 67 | 0.8% | 0% |
| Particulates | 42 | 0.5% | 0% |
| Loose or intermittent connection | 37 | 0.4% | 0.2% |
| Failure to deliverthe device did not deliver the dose or item | 36 | 0.4% | 0.8% |
| Product quality problem | 26 | 0.3% | 0% |
| Failure to prime | 25 | 0.3% | 0% |
| Burst container or vessel | 23 | 0.3% | 0% |
| Insufficient flow or under infusion | 23 | 0.3% | 0.8% |
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 | 6,726 | 81.4% |
| Underdoseless than the intended dose | 13 | 0.2% |
| Injurya physical injury | 4 | 0% |
| Anaphylactic shocka severe allergic reaction with collapse | 1 | 0% |
| Anxietyanxiety | 1 | 0% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 1 | 0% |
| Dyspneashortness of breath | 1 | 0% |
| Hypersensitivity/allergic reaction | 1 | 0% |
| Internal organ perforation | 1 | 0% |
| Nauseafeeling sick | 1 | 0% |
| Overdosea dose above the recommended amount | 1 | 0% |
| Painpain, site not specified | 1 | 0% |
| Palpitationsawareness of the heartbeat | 1 | 0% |
| Tinnitusringing in the ears | 1 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Intermate | Product code FRN | All MAUDE reports |
|---|---|---|---|
| Reports | 8,261 | 1,831,109 | 26,136,888 |
| Share of that pool | — | 0.5% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 0.1% | 1.3% | 36.2% |
| Classified as malfunction | 99.9% | 98.5% | 62.3% |
| Filed by the manufacturer | 99.9% | 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 Pump Module | 684,522 | 0 | 0% |
| 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% |
| 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 Intermate reports
How many FDA reports name Intermate?
8,261 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 47 in the latest 12 months.
What kinds of events are reported?
malfunction (99.9%) and injury (0.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device contamination with chemical or other material (55.7%), material rupture (12.5%), component missing (6.5%), fluid/blood leak (5.5%) and break (4.9%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%) and voluntary reports (0.1%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Intermate 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.