Lutronic Corporation recalls
Every recall we track for Lutronic Corporation — 3 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Lutronic Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 2 | 0 | 0 | 2 |
What to do if you have a recalled Lutronic Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Lutronic Corporation recalls
3 shown- Use cautionMedical device
Lutronic Corporation recalls Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy
Lutronic recalls DermaV Medical laser devices with specific serial numbers due to potential patient burns from spark/loud noise during high-fluence treatments at 1064nm wavelength.
LutronicAug 6, 2026 - Use cautionMedical device
Lutronic Corporation recalls CLARITY II Laser System; Model No. 1110200210.
Lutronic recalls CLARITY II Laser System model 1110200210 due to reports of sparking and potential patient burns. Affected units have specific serial numbers listed in the recall notice.
LutronicJan 27, 2026 - Lower riskMedical device
Lutronic Corporation recalls XERF EFFECTOR 60. Electrosurgical unit.
Lutronic recalls XERF EFFECTOR 60 electrosurgical units made between April 2025 and August 2025 due to rare patient adverse events from manufacturing defects.
LutronicSep 4, 2025
Lutronic Corporation recall questions
How many recalls has Lutronic Corporation had?
3 recalls from Lutronic Corporation are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Lutronic Corporation recall?
Lutronic Corporation recalls Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy, dated Aug 6, 2026. Every Lutronic Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Lutronic Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Lutronic Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.