Device brand name · Surgical irrigation/aspiration cannula non-illuminating single-use
Elefant suction-irrigation device: medical device reports filed with FDA
290 reports name it, 2023–2026. Manufacturer given most often on reports: Coloplast A/S. Product code FQH.
- 290
- device reports naming the brand
- 0% of all MAUDE reports · about 92 a year
- 182
- reports, 12 months to August 2026
- 104 in the 12 months before
- 100%
- classified as malfunction
- 92.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
290 medical device reports received by FDA name the brand "Elefant suction-irrigation device" (surgical irrigation/aspiration cannula non-illuminating single-use); the manufacturer given most often on reports is Coloplast A/S; received from May 2023 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
182 reports arrived in the 12 months to August 2026, up 75% from 104 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 (100%); across all lavage, jet reports (product code FQH) death is recorded in 0.1% and malfunction in 92.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are suction failure (92.8%), inability to irrigate (87.2%) and suction problem (1%). The patient problems coded most often are foreign body in patient. 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 4,932 reports carrying product code FQH. 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 |
|---|---|---|---|
| Suction failure | 269 | 92.8% | 5.6% |
| Inability to irrigate | 253 | 87.2% | 9.4% |
| Suction problem | 3 | 1% | 0.4% |
| Device misassembled during manufacturing /shipping | 2 | 0.7% | 0% |
| Fluid/blood leak | 1 | 0.3% | 3.7% |
| Free or unrestricted flow | 1 | 0.3% | 0% |
| Inaccurate delivery | 1 | 0.3% | 0.4% |
| Material separation | 1 | 0.3% | 0.4% |
| Missing information | 1 | 0.3% | 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 |
|---|---|---|
| Foreign body in patientpart of a device left in the patient | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Elefant suction-irrigation device | Product code FQH | All MAUDE reports |
|---|---|---|---|
| Reports | 290 | 4,932 | 26,136,888 |
| Share of that pool | — | 5.9% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 0% | 6.7% | 36.2% |
| Classified as malfunction | 100% | 92.6% | 62.3% |
| Filed by the manufacturer | 100% | 95.2% | 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 FQH
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Fan Spray Kit | 850 | 173 | 0% |
| Hip Kit | 652 | 135 | 0% |
| BD Surgiphor Sterile Wound Irrigation System | 268 | 101 | 0% |
| Versajet Exact Assy 45 Degree X 14mm | 150 | 4 | 0% |
| Zimmer Skin Graft Mesher | 3,463 | 285 | 0% |
| Renasys Touch Device & Power Sup | 447 | 0 | 0% |
| Stryker | 559 | 5 | 1.3% |
| Zimmer Air Dermatome | 2,687 | 372 | 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 Elefant suction-irrigation device reports
How many FDA reports name Elefant suction-irrigation device?
290 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 182 in the latest 12 months.
What kinds of events are reported?
malfunction (100%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
suction failure (92.8%), inability to irrigate (87.2%), suction problem (1%), device misassembled during manufacturing /shipping (0.7%) and fluid/blood leak (0.3%). 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 Elefant suction-irrigation device 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.