Elastic UV-Absorbing Silicone Posterior Chamber Intraocular Lens - Toric Optic AA4203TL (UDI 00841542100762)Recalls & reported problems
Staar Surgical Company · Diopter: 20.5 SE/2.0 Toric; Overall Diameter (Length): 11.2 mm (Longer Haptic) · 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 00841542100762), received between Mar 2, 2017 and Mar 2, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (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
- Patient-Device Incompatibility1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 2, 2017Patient-Device Incompatibility; Patient-Device Incompatibility
THE REPORTER STATED THAT THE SURGEON IMPLANTED AND EXPLANTED AN (B)(4) TORIC LENS, 20.5 DIOPTER, ON THE SAME DAY AND REPLACED IT WITH A DIFFERENT LENS. THE REPORTER STATED THAT THE SURGEON WAS NOT SATISFIED HOW THE LENS SAT ON THE CAPSULAR BAG. THE INCISION WAS ENLARGED TO REMOVE THE LENS AND SUTURE WERE USED. THERE WAS NO PATIENT INJURY .
Patient problems: No Code Available
MAUDE report 6373480 ↗
Other Lens, Intraocular, Toric Optics devices
- TECNIS IOL ZCT150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS1 recall7 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS43 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS36 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS32 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS30 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS29 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS21 reports
- TECNIS IOL DIU150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS19 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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