Device brand name · Lavage jet
Hip Kit: medical device reports filed with FDA
652 reports name it, 2016–2026. Manufacturer given most often on reports: Zimmer Surgical. Product code FQH.
- 652
- device reports naming the brand
- 0% of all MAUDE reports · about 63 a year
- 135
- reports, 12 months to August 2026
- 192 in the 12 months before
- 96.8%
- classified as malfunction
- 92.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 652 reports that name the brand "Hip Kit" (lavage jet), received between February 2016 and August 2026; the manufacturer given most often on reports is Zimmer Surgical. Spellings of one product vary from report to report.
135 reports arrived in the 12 months to August 2026, down 30% from 192 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 (96.8%) and injury (3.2%); 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 inability to irrigate (16.9%), battery problem (13.5%) and delivered as unsterile product (13.2%). The patient problems coded most often are no patient involvement, foreign body in patient and device embedded in tissue or plaque. 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 |
|---|---|---|---|
| Inability to irrigate | 110 | 16.9% | 9.4% |
| Battery problema problem with the battery | 88 | 13.5% | 5.5% |
| Delivered as unsterile product | 86 | 13.2% | 9% |
| Detachment of device or device componentpart of the device came off | 45 | 6.9% | 4.9% |
| Overheating of device | 45 | 6.9% | 5.5% |
| Expulsion | 39 | 6% | 2.3% |
| Failure to power up | 35 | 5.4% | 2.6% |
| Device contaminated during manufacture or shipping | 34 | 5.2% | 2.5% |
| Mechanical problema mechanical problem | 34 | 5.2% | 2.6% |
| Explosion | 25 | 3.8% | 1.5% |
| Disconnection | 24 | 3.7% | 1.2% |
| Powder leak | 23 | 3.5% | 1% |
| Fluid/blood leak | 21 | 3.2% | 3.7% |
| Activation problem | 18 | 2.8% | 0.8% |
| Leak/splashthe device leaked | 15 | 2.3% | 3.8% |
| Pressure problem | 15 | 2.3% | 1.1% |
| Corrodedthe device corroded | 12 | 1.8% | 1.4% |
| Melted | 12 | 1.8% | 0.9% |
| Manufacturing, packaging or shipping problem | 11 | 1.7% | 1% |
| Power problem | 10 | 1.5% | 0.5% |
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 | 22 | 3.4% |
| Foreign body in patientpart of a device left in the patient | 17 | 2.6% |
| Device embedded in tissue or plaque | 2 | 0.3% |
| Burn(s)a burn | 1 | 0.2% |
| Eye injury | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Hip Kit | Product code FQH | All MAUDE reports |
|---|---|---|---|
| Reports | 652 | 4,932 | 26,136,888 |
| Share of that pool | — | 13.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 3.2% | 6.7% | 36.2% |
| Classified as malfunction | 96.8% | 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% |
| Elefant suction-irrigation device | 290 | 182 | 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 Hip Kit reports
How many FDA reports name Hip Kit?
652 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 135 in the latest 12 months.
What kinds of events are reported?
malfunction (96.8%) and injury (3.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
inability to irrigate (16.9%), battery problem (13.5%), delivered as unsterile product (13.2%), detachment of device or device component (6.9%) and overheating of device (6.9%). 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 Hip Kit 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.