Device brand name · Infusion pump
Omni-Flow Model 4000 Plus: medical device reports filed with FDA
225 reports name it, 1998–2008. Manufacturer given most often on reports: Abbott Laboratories. Product code FRN.
- 225
- device reports naming the brand
- 0% of all MAUDE reports · about 8 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 85.8%
- classified as malfunction
- 98.5% across the product code
- 1.8%
- classified as death, as reported
- 4 reports · not verified by FDA
FDA's MAUDE database holds 225 reports that name the brand "Omni-Flow Model 4000 Plus" (infusion pump), received between May 1998 and December 2008; the manufacturer given most often on reports is Abbott Laboratories. 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 (85.8%), injury (9.3%) and other (2.7%); 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 (24%), replace (13.3%) and no audible alarm (11.1%). The patient problems coded most often are no patient involvement, overmedicated and therapy/non-surgical treatment/delayed/prolonged. 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
No report naming Omni-Flow Model 4000 Plus was received in the five years to August 2026; the latest was received in December 2008.
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 | 54 | 24% | 1.2% |
| Replace | 30 | 13.3% | 0.1% |
| No audible alarm | 25 | 11.1% | 0.2% |
| Occlusion within devicethe device blocked | 19 | 8.4% | 0.6% |
| Alarm, audible | 17 | 7.6% | 0.1% |
| Overdelivery | 17 | 7.6% | 0.1% |
| Device alarm system | 13 | 5.8% | 2.8% |
| Loss of powerthe device lost power | 13 | 5.8% | 0.1% |
| Failure to deliverthe device did not deliver the dose or item | 12 | 5.3% | 0.8% |
| Failure to infuse | 12 | 5.3% | 0.4% |
| Insufficient flow or under infusion | 10 | 4.4% | 0.8% |
| Device displays incorrect message | 9 | 4% | 9.3% |
| Device, removal of (non-implant) | 8 | 3.6% | 0% |
| Underdelivery | 8 | 3.6% | 0.1% |
| Inaccurate delivery | 7 | 3.1% | 0.4% |
| Output above specifications | 7 | 3.1% | 0% |
| Pressure sensor failure | 6 | 2.7% | 0% |
| Battery failure | 4 | 1.8% | 0.2% |
| Device issuea problem with the device | 3 | 1.3% | 0.1% |
| Failure to pump | 3 | 1.3% | 0.1% |
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 | 26 | 11.6% |
| Overmedicated | 20 | 8.9% |
| Therapy/non-surgical treatment/delayed/prolonged | 20 | 8.9% |
| Treatment with medication(s) | 15 | 6.7% |
| Blood pressure, decreased | 14 | 6.2% |
| Therapy/non-surgical treatment, additional | 13 | 5.8% |
| Therapy/non-surgical treatment, aborted/stopped | 9 | 4% |
| Blood pressure, low | 8 | 3.6% |
| Underdoseless than the intended dose | 8 | 3.6% |
| Deaththe patient died; cause not stated by this term | 5 | 2.2% |
| Low blood pressure/ hypotension | 5 | 2.2% |
| Overdosea dose above the recommended amount | 4 | 1.8% |
| Blood pressure, high | 3 | 1.3% |
| Blood pressure, increased | 3 | 1.3% |
| Resuscitation | 3 | 1.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Omni-Flow Model 4000 Plus | Product code FRN | All MAUDE reports |
|---|---|---|---|
| Reports | 225 | 1,831,109 | 26,136,888 |
| Share of that pool | — | 0% | 0% |
| Classified as death, per 1,000 reports | 18 | 1 | 9 |
| Classified as injury | 9.3% | 1.3% | 36.2% |
| Classified as malfunction | 85.8% | 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 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 Omni-Flow Model 4000 Plus reports
How many FDA reports name Omni-Flow Model 4000 Plus?
225 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 (85.8%), injury (9.3%) and other (2.7%). "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 (24%), replace (13.3%), no audible alarm (11.1%), occlusion within device (8.4%) and alarm, audible (7.6%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Omni-Flow Model 4000 Plus 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.