ACRYSOF® ACRYSERT® SN6CWS (REF SN6CWS.205)Recalls & reported problems
Alcon Laboratories, Inc. · AcrySof(R) IQ ASPHERIC IOL, SP ACRYLIC FOLDABLELENS, w/AcrySert(R) DELIVERY SYSTEM, UV w/BLUELIGHT FILTER, 13.0mm LENGTH, 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS. · 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 00380652249225), received between Oct 17, 2023 and Oct 17, 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Corneal Edema1
- Uveitis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 17, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A NON-HEALTHCARE PROFESSIONAL REPORTED VIA CHINEES HEALTH AUTHORITY THAT, FOLLOWING THE CATARACT SURGERY WITH INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT WAS DIAGNOSED WITH POSTOPERATIVE ANTERIOR UVEITIS. ON THE FIRST POSTOPERATIVE WARD VISIT, IT WAS FOUND THAT THE PATIENT'S CORNEA HAD FOGGY EDEMA, WITH KP+ANTERIOR CLEARANCE, CELLS++, AND ATRIAL SCINTILLATION++. A SMALL AMOUNT OF EXUDATE FILM WAS VISIBLE IN THE PUPIL AREA, AND THE IOL WAS IN PLACE. THE PATIENT WAS ADVISED TO ADMINISTER TOBRAMYCIN DEXAMETHASONE EYE DROPS AND BROMFENAC SODIUM EYE DROPS EVERY 10 MINUTES. AFTER ANTI-INFLAMMATORY AND ANTI IMMUNE TREATMENT, THE INFLAMMATORY RESPONSE SUBSIDED. IT WAS REPORTED THAT THE EVENTS HAPPENED DUE TO PATIENT'S OWN REASONS.
Patient problems: Corneal Edema; Uveitis
MAUDE report 17948949 ↗
Other intraocular lens devices
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- 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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