Multiflex MTA3U0 (REF MTA3U0.110)Recalls & reported problems
Alcon Laboratories, Inc. · MULTIFLEX(TM*)III SINGLE-PIECE PMMASTERILE ACL (IOL/AC), 12.5mm LENGTH, 5.5mmCONVEXOPLANO OPTIC, 0.5mm VAULTED HAPTICS. *REG. U.S. PAT. & TM OFF. · Class 3 · Implant
All models of Multiflex (28)
Data updated Oct 16, 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 00380650701107), received between Jul 7, 2022 and Jul 7, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
Patient problems
- Visual Impairment1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 7, 2022Use of Device Problem; Use of Device Problem
A CONSUMER REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, HE HAD A HAD A POOR RESULT. THERE ARE CONCERNS THAT THE WHITE-TO-WHITE MEASUREMENT WAS TAKEN INCORRECTLY LEADING TO THE INSERTION OF THE WRONG SIZE LENS. THE CLIENT NOTES THAT WHITE-WHITE MEASUREMENTS SHOULD BE TAKEN PRIOR TO LENS INSERTION AND SHOULD BE TAKEN HORIZONTALLY, NOT VERTICALLY ADDITIONAL INFORMATION WAS REQUESTED AND RECEIVED THAT THE LENS WAS TOO BIG AND HAD TO BE REPLACED. IT WAS REPLACED IN (B)(6) 2019 AND HE HAS ALSO UNDERGONE A CORNEAL GRAFT. THE REPORT SEEMS TO BE COMING FROM A LEGAL ENTITY. THE IOL PROVIDED MIGHT BE THE FIRST ONE IMPLANTED; ASSUMING THAT THE CLIENT/PATIENT WOULD RATHER GIVE TO HIS LEGAL, DETAILS OF THE IOL THAT CAUSED THE CLAIM ON THE FIRST PLACE.
Patient problems: Visual Impairment
MAUDE report 14946011 ↗
Other intraocular lens devices
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens146 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens145 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens144 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens139 reports
- TECNIS SIMPLICITY DIB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens1 recall81 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens129 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens127 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens126 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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