Device brand name · Syringe pump
Perfusor Space: medical device reports filed with FDA
429 reports name it, 2009–2026. Manufacturer given most often on reports: B Braun Melsungen. Product code FRN.
- 429
- device reports naming the brand
- 0% of all MAUDE reports · about 25 a year
- 8
- reports, 12 months to August 2026
- 0 in the 12 months before
- 92.1%
- classified as malfunction
- 98.5% across the product code
- 2.1%
- classified as death, as reported
- 9 reports · not verified by FDA
429 medical device reports received by FDA name the brand "Perfusor Space" (syringe pump); the manufacturer given most often on reports is B Braun Melsungen; received from July 2009 to July 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
8 reports arrived in the 12 months to August 2026, with 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 (92.1%), injury (4.2%) and death (2.1%); 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 excess flow or over-infusion (33.1%), infusion or flow problem (32.2%) and insufficient flow or under infusion (15.6%). The patient problems coded most often are overdose, high blood pressure/ hypertension 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 |
|---|---|---|---|
| Excess flow or over-infusion | 142 | 33.1% | 1.2% |
| Infusion or flow problema problem with flow or infusion | 138 | 32.2% | 0.3% |
| Insufficient flow or under infusion | 67 | 15.6% | 0.8% |
| Inaccurate flow rate | 54 | 12.6% | 0.1% |
| Device alarm system | 32 | 7.5% | 2.8% |
| Improper flow or infusion | 21 | 4.9% | 0.5% |
| Pumping stopped | 18 | 4.2% | 0.2% |
| Pumping problem | 14 | 3.3% | 0% |
| Free or unrestricted flow | 7 | 1.6% | 0.1% |
| No audible alarm | 7 | 1.6% | 0.2% |
| Display or visual feedback problem | 6 | 1.4% | 1.1% |
| Failure to deliverthe device did not deliver the dose or item | 4 | 0.9% | 0.8% |
| Partial blockage | 4 | 0.9% | 0% |
| Device operates differently than expectedthe device behaved unexpectedly | 3 | 0.7% | 0.9% |
| Mechanical problema mechanical problem | 3 | 0.7% | 0.3% |
| Breakthe device broke | 2 | 0.5% | 8.5% |
| Device operational issue | 2 | 0.5% | 0% |
| Electrical /electronic property probleman electrical or electronic problem | 2 | 0.5% | 0.8% |
| Fail-safe problem | 2 | 0.5% | 0% |
| Fire | 2 | 0.5% | 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 |
|---|---|---|
| Overdosea dose above the recommended amount | 18 | 4.2% |
| High blood pressure/ hypertension | 10 | 2.3% |
| Low blood pressure/ hypotension | 9 | 2.1% |
| Hemorrhage/blood loss/bleeding | 8 | 1.9% |
| Tachycardiafast heart rate | 8 | 1.9% |
| Cardiac arrestthe heart stopped | 7 | 1.6% |
| Distress | 6 | 1.4% |
| Respiratory arrestbreathing stopped | 3 | 0.7% |
| Underdoseless than the intended dose | 3 | 0.7% |
| Loss of consciousnesspassing out | 2 | 0.5% |
| Apnea | 1 | 0.2% |
| Bradycardiaslow heart rate | 1 | 0.2% |
| Cognitive changes | 1 | 0.2% |
| Discomfortdiscomfort | 1 | 0.2% |
| Hypoglycemialow blood sugar | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Perfusor Space | Product code FRN | All MAUDE reports |
|---|---|---|---|
| Reports | 429 | 1,831,109 | 26,136,888 |
| Share of that pool | — | 0% | 0% |
| Classified as death, per 1,000 reports | 21 | 1 | 9 |
| Classified as injury | 4.2% | 1.3% | 36.2% |
| Classified as malfunction | 92.1% | 98.5% | 62.3% |
| Filed by the manufacturer | 89.7% | 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% |
| Intermate | 8,261 | 47 | 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 Perfusor Space reports
How many FDA reports name Perfusor Space?
429 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 8 in the latest 12 months.
What kinds of events are reported?
malfunction (92.1%), injury (4.2%) and death (2.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
excess flow or over-infusion (33.1%), infusion or flow problem (32.2%), insufficient flow or under infusion (15.6%), inaccurate flow rate (12.6%) and device alarm system (7.5%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (89.7%) and distributor reports (10%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Perfusor Space 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.