Device brand name · Arthroscope and accessories
Dw Arthroscopy Fluid Management Dev: medical device reports filed with FDA
1,053 reports name it, 2019–2026. Manufacturer given most often on reports: Arthrex. Product code HRX.
- 1,053
- device reports naming the brand
- 0% of all MAUDE reports · about 142 a year
- 158
- reports, 12 months to August 2026
- 168 in the 12 months before
- 91.5%
- classified as malfunction
- 87% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
1,053 medical device reports received by FDA name the brand "Dw Arthroscopy Fluid Management Dev" (arthroscope and accessories); the manufacturer given most often on reports is Arthrex; received from February 2019 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
158 reports arrived in the 12 months to August 2026, close to the 168 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 (91.5%) and injury (8.5%); across all arthroscope reports (product code HRX) death is recorded in 0.1% and malfunction in 87%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are pressure problem (20.1%), increase in pressure (12.9%) and defective device (7.9%). The patient problems coded most often are swelling/ edema, extravasation and appropriate clinical signs, symptoms and conditions term/code not available. 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 25,683 reports carrying product code HRX. 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 |
|---|---|---|---|
| Pressure problem | 212 | 20.1% | 2.3% |
| Increase in pressure | 136 | 12.9% | 4.5% |
| Defective devicethe device was defective | 83 | 7.9% | 0.8% |
| Infusion or flow problema problem with flow or infusion | 77 | 7.3% | 1.8% |
| Suction failure | 61 | 5.8% | 1.1% |
| Intermittent loss of power | 48 | 4.6% | 0.5% |
| No flow | 35 | 3.3% | 0.3% |
| Unexpected shutdown | 30 | 2.8% | 0.2% |
| Excess flow or over-infusion | 29 | 2.8% | 1.4% |
| Key or button unresponsive/not working | 25 | 2.4% | 0.2% |
| Pumping problem | 25 | 2.4% | 0.2% |
| Improper flow or infusion | 22 | 2.1% | 1.8% |
| Breakthe device broke | 17 | 1.6% | 12.5% |
| Suction problem | 17 | 1.6% | 0.4% |
| Decrease in pressure | 16 | 1.5% | 0.2% |
| Display or visual feedback problem | 16 | 1.5% | 4.3% |
| Erratic or intermittent display | 13 | 1.2% | 0.1% |
| Insufficient flow or under infusion | 11 | 1% | 0.1% |
| Noise, audible | 11 | 1% | 0.8% |
| Output problem | 9 | 0.9% | 1.6% |
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 |
|---|---|---|
| Swelling/ edema | 55 | 5.2% |
| Extravasation | 38 | 3.6% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 7 | 0.7% |
| Swellingswelling | 4 | 0.4% |
| Inflammationinflammation | 3 | 0.3% |
| Loss of range of motion | 3 | 0.3% |
| Pneumothoraxa collapsed lung | 3 | 0.3% |
| Edemaswelling from fluid | 2 | 0.2% |
| Failure of implant | 2 | 0.2% |
| Joint dislocationa dislocated joint | 2 | 0.2% |
| Painpain, site not specified | 2 | 0.2% |
| Bone cement implantation syndrome | 1 | 0.1% |
| Compartment syndrome | 1 | 0.1% |
| Deformity/ disfigurement | 1 | 0.1% |
| Exposure to body fluids | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Dw Arthroscopy Fluid Management Dev | Product code HRX | All MAUDE reports |
|---|---|---|---|
| Reports | 1,053 | 25,683 | 26,136,888 |
| Share of that pool | — | 4.1% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 8.5% | 10.6% | 36.2% |
| Classified as malfunction | 91.5% | 87% | 62.3% |
| Filed by the manufacturer | 99.9% | 94.9% | 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 HRX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Micro Tornado Hp W Handcontrol | 1,501 | 46 | 0% |
| METRx System | 1,679 | 267 | 0.1% |
| Fms Vue Pump | 706 | 37 | 0% |
| Hd Epscp 4 0 30 167 Mitek | 575 | 27 | 0% |
| 4k C-Mnt Scp 4 0 30 167 Mitek | 541 | 205 | 0% |
| Cordless Driver 3 | 476 | 0 | 0% |
| Dii Controller | 354 | 6 | 0% |
| Shaver Handpiece 2 0 With Buttons | 329 | 87 | 0% |
| 4580 Fms Duo+ Pump/Shaver Combo -Ns | 316 | 2 | 0% |
| Kyphon Xpander Inflatable Bone Tamp | 315 | 22 | 0% |
| Sagittal Saw Attachment | 1,505 | 64 | 0% |
| Control Unit Dyonics 25 | 287 | 41 | 0% |
| Fms Tornado Micro Handpiece With Buttons | 285 | 0 | 0% |
| Vapr3 Footswitch Ea | 243 | 2 | 0% |
| Inflow Tubing Fms Vue 24pk | 226 | 22 | 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 Dw Arthroscopy Fluid Management Dev reports
How many FDA reports name Dw Arthroscopy Fluid Management Dev?
1,053 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 158 in the latest 12 months.
What kinds of events are reported?
malfunction (91.5%) and injury (8.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
pressure problem (20.1%), increase in pressure (12.9%), defective device (7.9%), infusion or flow problem (7.3%) and suction failure (5.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Dw Arthroscopy Fluid Management Dev 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.