AcrySof™ IQ Vivity™ DFT015 (REF DFT015.270)Recalls & reported problems
Alcon Laboratories, Inc. · Sterile UV and Blue Light Filtering Acrylic Foldable Aspheric Wavefront-Shaping Posterior Chamber Intraocular Lens · Class 3 · Implant
All models of AcrySof IQ Vivity (225)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00380652421379), received between Apr 10, 2023 and Apr 10, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Scratched Material” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Scratched Material1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 10, 2023Scratched Material; Scratched Material
A OTHER HEALTH CARE PROFESSIONAL REPORTED THAT DURING AN INTRAOCULAR LENS IOL IMPLANT PROCEDURE, SURGEON NOTICED IN MICROSCOPE THAT THERE WAS A MARK ON THE IOL SURFACE FROM THE EDGE TOWARDS THE CENTER OF THE OPTICS, THE MARK WAS SERPENTINE SHAPED AND LOOKED LIKE A FIBER. THE SURGEON MADE SURE THAT IT WAS NOT A FIBER BUT A MARK ON THE OPTICS. THE IOL WAS LEFT IN THE PATIENTS EYE. PATIENT IS COMING BACK AFTER 4 WEEKS AND THEY ARE THEN CONSIDERING THE POSSIBLE HARM TO PATIENT. THE REPORTER DOES NOT AGREED FOR FURTHER INFORMATION.
Patient problems: Insufficient Information
MAUDE report 16708377 ↗
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- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens73 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens71 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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