Akreos® IOL AO60 (REF AO60P2050)Recalls & reported problems
Bausch & Lomb Incorporated · Akreos Advanced Optics Aspheric Lens +20.50D · Class 3 · Implant
All models of Akreos IOL (8)
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 10757770502063), received between Aug 29, 2025 and Aug 29, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Calcified” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Calcified1
- Device Dislodged or Dislocated1
Patient problems
- Blurred Vision1
- Calcium Deposits/Calcification1
- Visual Disturbances1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 29, 2025Calcified; Device Dislodged or Dislocated; Calcified; Device Dislodged or Dislocated
IT WAS REPORTED THAT APPROXIMATELY 6 YEARS AFTER IMPLANTATION OF AN INTRAOCULAR LENS (IOL), THE PATIENT NOTICED A DECREASE OF VISION AND FUZZINESS IN THEIR LEFT EYE. THE SURGEON'S FINDINGS WERE A CALCIFIED LENS WITH AGAINST THE RULE ASTIGMATISM. APPROXIMATIVELY 4 MONTHS LATER, THE LENS WAS EXCHANGED FOR A DIFFERENT MODEL IOL DUE TO DISLOCATION. A VITRECTOMY WAS PERFORMED DUE TO VITREOUS STRANDS. IN THE SURGEON¿S OPINION THE LIKELY CAUSE OF THE IOL DISLOCATION WAS THE CALCIFICATION OF THE LENS. THE PATIENT¿S OUTCOME IS GOOD.
Patient problems: Blurred Vision; Calcium Deposits/Calcification; Visual Disturbances
MAUDE report 22923215 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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