Akreos AOP IOL ADAPTAOP2950Recalls & reported problems
Bausch & Lomb Incorporated · ADAPT-AOP 10.5MM +29.50 · 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 10757770486158), received between Dec 22, 2020 and Dec 22, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- No Code Available1
- Visual Impairment1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
ADDITIONAL INFORMATION WAS LOCATED IN AN ARTICLE TITLED "POST CATARACT SURGERY REFRACTIVE SURPRISE DUE TO INTRAOCULAR LENS MISLABELING" RELATING TO THIS EVENT. IT WAS REPORTED THAT THE ORIGINAL SURGICAL PROCEDURE TYPE WAS PHACOEMULSIFICATION WITH POSTERIOR CHAMBER IOL IMPLANTATION AND VISCO-GONIO-SYNECHIA-LYSIS. THE POST REPLACEMENT SURGERY VISION WAS STABLE AT 1- AND 3-MONTH APPOINTMENTS.
Patient problems: No Code Available; Visual Impairment
MAUDE report 11057753 ↗
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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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