Device brand name · Attune instruments handles
Attune Impaction Handle: medical device reports filed with FDA
1,975 reports name it, 2012–2026. Manufacturer given most often on reports: Depuy Ireland - 9616671. Product code HWA.
- 1,975
- device reports naming the brand
- 0% of all MAUDE reports · about 137 a year
- 64
- reports, 12 months to August 2026
- 128 in the 12 months before
- 99.2%
- classified as malfunction
- 98% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
1,975 medical device reports received by FDA name the brand "Attune Impaction Handle" (attune instruments handles); the manufacturer given most often on reports is Depuy Ireland - 9616671; received from February 2012 to June 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
64 reports arrived in the 12 months to August 2026, down 50% from 128 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 (99.2%) and injury (0.8%); across all impactor reports (product code HWA) death is recorded in 0% and malfunction in 98%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are break (93.4%), device-device incompatibility (2.3%) and crack (1.2%). The patient problems coded most often are not applicable, no patient involvement and pain. 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 19,425 reports carrying product code HWA. 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 |
|---|---|---|---|
| Breakthe device broke | 1,844 | 93.4% | 69.8% |
| Device-device incompatibility | 46 | 2.3% | 6% |
| Crackthe device cracked | 24 | 1.2% | 8% |
| Detachment of device or device componentpart of the device came off | 16 | 0.8% | 0.6% |
| Naturally worn | 15 | 0.8% | 5.2% |
| Contamination /decontamination problem | 11 | 0.6% | 1.4% |
| Material integrity problema problem with the device material | 8 | 0.4% | 0.8% |
| Fracturea broken bone | 7 | 0.4% | 6.1% |
| Insufficient device problem information | 5 | 0.3% | 0.2% |
| Material twisted/bent | 5 | 0.3% | 1.7% |
| Device contamination with chemical or other material | 4 | 0.2% | 0.1% |
| Component missing | 3 | 0.2% | 0.3% |
| Unintended movement | 3 | 0.2% | 0.5% |
| Connection problema connection problem | 2 | 0.1% | 0.2% |
| Device dislodged or dislocated | 2 | 0.1% | 0% |
| Disassembly | 2 | 0.1% | 0.2% |
| Material deformation | 2 | 0.1% | 3.8% |
| Mechanical jam | 2 | 0.1% | 0.7% |
| Scratched material | 2 | 0.1% | 1.2% |
| Bent | 1 | 0.1% | 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 |
|---|---|---|
| Not applicable | 15 | 0.8% |
| No patient involvement | 2 | 0.1% |
| Painpain, site not specified | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Attune Impaction Handle | Product code HWA | All MAUDE reports |
|---|---|---|---|
| Reports | 1,975 | 19,425 | 26,136,888 |
| Share of that pool | — | 10.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 0.8% | 1.8% | 36.2% |
| Classified as malfunction | 99.2% | 98% | 62.3% |
| Filed by the manufacturer | 99.9% | 99.5% | 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 HWA
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Pinn Straight Cup Impactor | 4,807 | 315 | 0% |
| Attune Femoral Impactor | 3,328 | 121 | 0% |
| Attune Fb Tibial Impactor | 1,954 | 114 | 0% |
| Attune Rp Tibial Impactor | 1,025 | 32 | 0% |
| Sp2 Tibial Radel Impactor | 1,039 | 2 | 0% |
| Duraloc Str Cup Impactor | 909 | 57 | 0% |
| Concave Impactor Tip | 342 | 18 | 0% |
| S/C Trial Handle Angled | 330 | 32 | 0% |
| Duraloc Curved Cup Impactor | 310 | 19 | 0% |
| Attune | 1,958 | 1,944 | 0% |
| Pinnacle | 689 | 499 | 0.1% |
| Sigma Hp Fbt Keel Punch Impact | 219 | 0 | 0% |
| Sigma Hp Fem Notch Impactor | 262 | 8 | 0% |
| Impactor F/Pfna Blade | 284 | 0 | 0% |
| Sp 2 Femoral Impactor | 246 | 2 | 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 Attune Impaction Handle reports
How many FDA reports name Attune Impaction Handle?
1,975 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 64 in the latest 12 months.
What kinds of events are reported?
malfunction (99.2%) and injury (0.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
break (93.4%), device-device incompatibility (2.3%), crack (1.2%), detachment of device or device component (0.8%) and naturally worn (0.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%) and voluntary reports (0.1%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Attune Impaction Handle 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.