Devices › Instrument, ultrasonic surgical
Device brand name · Instrument ultrasonic surgical
Tx2 Tissue Removal System - Microtip: medical device reports filed with FDA
308 reports name it, 2017–2025. Manufacturer given most often on reports: Tenex Health. Product code LFL.
- 308
- device reports naming the brand
- 0% of all MAUDE reports · about 35 a year
- 0
- reports, 12 months to August 2026
- 5 in the 12 months before
- 80.8%
- classified as malfunction
- 94.9% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
308 medical device reports received by FDA name the brand "Tx2 Tissue Removal System - Microtip" (instrument ultrasonic surgical); the manufacturer given most often on reports is Tenex Health; received from October 2017 to May 2025. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, against 5 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 (80.8%) and injury (19.2%); across all instrument, ultrasonic surgical reports (product code LFL) death is recorded in 0.1% and malfunction in 94.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are fracture (81.5%), break (13%) and detachment of device component (9.1%). The patient problems coded most often are foreign body in patient, pain 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 68,457 reports carrying product code LFL. 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 |
|---|---|---|---|
| Fracturea broken bone | 251 | 81.5% | 1.1% |
| Breakthe device broke | 40 | 13% | 20.5% |
| Detachment of device component | 28 | 9.1% | 6.9% |
| Component falling | 5 | 1.6% | 3.9% |
| Device dislodged or dislocated | 3 | 1% | 0.2% |
| Insufficient device problem information | 3 | 1% | 1.2% |
| Material separation | 3 | 1% | 11% |
| Detachment of device or device componentpart of the device came off | 1 | 0.3% | 6.8% |
| Disconnection | 1 | 0.3% | 0.1% |
| Material fragmentation | 1 | 0.3% | 0.3% |
| Overheating of device | 1 | 0.3% | 1.2% |
| Temperature problem | 1 | 0.3% | 0.2% |
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 | 6 | 1.9% |
| Painpain, site not specified | 6 | 1.9% |
| Device embedded in tissue or plaque | 5 | 1.6% |
| Swelling/ edema | 3 | 1% |
| Burn(s)a burn | 2 | 0.6% |
| Burn, thermal | 2 | 0.6% |
| Hematomaa collection of blood under the skin or in tissue | 2 | 0.6% |
| No patient involvement | 2 | 0.6% |
| Inadequate pain relief | 1 | 0.3% |
| Inflammationinflammation | 1 | 0.3% |
| Nerve damage | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Tx2 Tissue Removal System - Microtip | Product code LFL | All MAUDE reports |
|---|---|---|---|
| Reports | 308 | 68,457 | 26,136,888 |
| Share of that pool | — | 0.4% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 19.2% | 4.5% | 36.2% |
| Classified as malfunction | 80.8% | 94.9% | 62.3% |
| Filed by the manufacturer | 100% | 96.8% | 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 LFL
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Ultracision Harmonic Ace | 9,358 | 0 | 0% |
| Harmonic Ace Plus 7 Adv Hemostasis 36 | 6,831 | 537 | 0% |
| Harmonic Hd 1000i Shears 36cm Shaft | 5,033 | 196 | 0% |
| Harmonic Lap 5mm Shear 36cm | 2,720 | 88 | 0% |
| Harmonic Ace 36 Cm | 2,598 | 0 | 0.1% |
| Harmonic Ace 36cm W Erg Handle | 2,341 | 0 | 0% |
| Sonicision | 1,809 | 139 | 0.2% |
| Harmonic Scalpel Ultracision Hand Piece | 1,677 | 0 | 0.1% |
| SONICBEAT 5 mm, 35 cm, Front-actuated Grip | 1,640 | 373 | 0% |
| Harmonic ACE | 1,636 | 680 | 0.1% |
| Harmonic 1100 Shears 36cm | 1,434 | 203 | 0.1% |
| Ultracision Harmonic Scalpel Hand Piece | 1,430 | 0 | 0% |
| Harmonic Scalpel Hand Piece | 1,365 | 23 | 0% |
| Ultracision Surg Dev Curved Shears Endo | 1,586 | 0 | 0% |
| Harmonic Scalpel Ultracision Laparosonic Coagulating She | 1,067 | 0 | 0.1% |
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 Tx2 Tissue Removal System - Microtip reports
How many FDA reports name Tx2 Tissue Removal System - Microtip?
308 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (80.8%) and injury (19.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fracture (81.5%), break (13%), detachment of device component (9.1%), component falling (1.6%) and device dislodged or dislocated (1%). 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 Tx2 Tissue Removal System - Microtip 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.