VICTUS™ Femtosecond Laser Platform 3.2Recalls & reported problems
Technolas Perfect Vision GmbH · The laser system is an ophthalmologic system based on femtosecond technology. It is used to treat a wide variety of ophthalmologic indications. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04050555002895), received between Sep 22, 2026 and Sep 22, 2026 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Capsular Bag Tear1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem
On (b)(6) 2026 the surgeon reported a Capsulotomy tag that lead to a tear. On (b)(6) 2026 additional information was received. The surgeon confirmed that parts of the crystalline lens dropped into the Vitreous, and that the patient has been referred to another clinic (this is the awareness date). After further inquiry on (b)(6) 2026 we received the information that the patient had the lens fragments removed and a posterior vitrectomy was performed.
Patient problems: Capsular Bag Tear
MAUDE report 50851380 ↗
Other Ophthalmic Femtosecond Laser devices
- LenSx 8065998162Alcon Laboratories, Inc. · Ophthalmic femtosecond laser599 reports
- CATALYS SYSTEM CATALYS-UOptimedica Corporation · Ophthalmic femtosecond laser576 reports
- WaveLight 8065990941Alcon Laboratories, Inc. · Ophthalmic femtosecond laser460 reports
- ALLY 70-00050-001LENSAR, Inc. · Ophthalmic Femtosecond Laser81 reports
- LIQUID OPTICS INTERFACE 0180-1201Johnson & Johnson Surgical Vision, Inc. · Ophthalmic femtosecond laser51 reports
- ELITA EL2022Johnson & Johnson Surgical Vision, Inc. · Ophthalmic femtosecond laser31 reports
- LIQUID OPTICS INTERFACE 0180-1401Johnson & Johnson Surgical Vision, Inc. · Ophthalmic femtosecond laser28 reports
- CATALYS SYSTEM CAT PREC LSR SYSJohnson & Johnson Surgical Vision, Inc. · Ophthalmic femtosecond laser14 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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