Device brand name · Pump infusion
CADD Solis Pump: medical device reports filed with FDA
162 reports name it, 2019–2026. Manufacturer given most often on reports: Smiths Medical Asd. Product code FRN.
- 162
- device reports naming the brand
- 0% of all MAUDE reports · about 24 a year
- 57
- reports, 12 months to August 2026
- 30 in the 12 months before
- 85.8%
- classified as malfunction
- 98.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 162 reports that name the brand "CADD Solis Pump" (pump infusion), received between November 2019 and August 2026; the manufacturer given most often on reports is Smiths Medical Asd. Spellings of one product vary from report to report.
57 reports arrived in the 12 months to August 2026, up 90% from 30 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 (10.5%) and other (3.1%); 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 alarm system (11.1%), failure to infuse (9.9%) and excess flow or over-infusion (4.9%). The patient problems coded most often are dizziness, headache and itching sensation. 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 alarm system | 18 | 11.1% | 2.8% |
| Failure to infuse | 16 | 9.9% | 0.4% |
| Excess flow or over-infusion | 8 | 4.9% | 1.2% |
| Obstruction of flow | 6 | 3.7% | 0.3% |
| Volume accuracy problem | 4 | 2.5% | 0.1% |
| Battery problema problem with the battery | 3 | 1.9% | 1.2% |
| Computer software problema software problem | 3 | 1.9% | 0.6% |
| Defective devicethe device was defective | 3 | 1.9% | 0% |
| Device sensing problem | 3 | 1.9% | 3.8% |
| Failure to deliverthe device did not deliver the dose or item | 3 | 1.9% | 0.8% |
| Failure to sense | 3 | 1.9% | 0.9% |
| Material integrity problema problem with the device material | 3 | 1.9% | 0% |
| Protective measures problem | 3 | 1.9% | 0.5% |
| Air/gas in device | 2 | 1.2% | 0.1% |
| Complete blockage | 2 | 1.2% | 0% |
| Component missing | 2 | 1.2% | 0.1% |
| Device displays incorrect message | 2 | 1.2% | 9.3% |
| Display or visual feedback problem | 2 | 1.2% | 1.1% |
| Failure to power up | 2 | 1.2% | 0.2% |
| Grounding malfunction | 2 | 1.2% | 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 |
|---|---|---|
| Dizzinesslight-headedness or unsteadiness | 3 | 1.9% |
| Headachehead pain | 3 | 1.9% |
| Itching sensation | 3 | 1.9% |
| Chest painchest pain | 2 | 1.2% |
| Dyspneashortness of breath | 2 | 1.2% |
| Hypersensitivity/allergic reaction | 2 | 1.2% |
| Nauseafeeling sick | 2 | 1.2% |
| Respiratory failurethe lungs could not supply enough oxygen | 2 | 1.2% |
| Swelling/ edema | 2 | 1.2% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 1 | 0.6% |
| Diarrhea | 1 | 0.6% |
| Heartburn/indigestion | 1 | 0.6% |
| Hypoxialow oxygen | 1 | 0.6% |
| Local reaction | 1 | 0.6% |
| Muscle weakness/atrophy | 1 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | CADD Solis Pump | Product code FRN | All MAUDE reports |
|---|---|---|---|
| Reports | 162 | 1,831,109 | 26,136,888 |
| Share of that pool | — | 0% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 10.5% | 1.3% | 36.2% |
| Classified as malfunction | 85.8% | 98.5% | 62.3% |
| Filed by the manufacturer | 69.8% | 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 CADD Solis Pump reports
How many FDA reports name CADD Solis Pump?
162 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 57 in the latest 12 months.
What kinds of events are reported?
malfunction (85.8%), injury (10.5%) and other (3.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device alarm system (11.1%), failure to infuse (9.9%), excess flow or over-infusion (4.9%), obstruction of flow (3.7%) and volume accuracy problem (2.5%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (69.8%) and voluntary reports (30.2%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that CADD Solis Pump 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.