Akreos AOP IOL ADAPTAOP0700Recalls & reported problems
Bausch & Lomb Incorporated · ADAPT-AOP 11.0MM +07.00 · Class 3 · Implant
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 10757770485731), received between Jul 20, 2023 and Jul 20, 2023 — 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Endophthalmitis1
- Eye Pain1
- 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 20, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT IS REPORTED THAT, ONE WEEK AFTER IMPLANTATION OF AN IOL, A PATIENT WAS FOUND TO HAVE VISUAL ACUITY LOSS, EYE PAIN, CONJUNCTIVAL CONGESTION, AND EDEMA, WHICH WAS LATER DIAGNOSED AS ENDOPHTHALMITIS. AFTER HOSPITALIZATION, THE SYMPTOMS IMPROVED, THE VISION RECOVERED, AND THE PATIENT WAS DISCHARGED. 10 DAYS POST-DISCHARGE A RE-EXAMINATION OF THE PATIENT SHOWED A RECURRENCE OF ENDOPHTHALMITIS. THE PATIENT WAS REFERRED TO ANOTHER HOSPITAL FOR FURTHER DIAGNOSIS AND TREATMENT.
Patient problems: Endophthalmitis; Eye Pain; Visual Impairment
MAUDE report 17365172 ↗
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- 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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