VERION™ 8065998269Recalls & reported problems
Alcon Laboratories, Inc. · VERION™ Digital Marker L · Class 1
All models of VERION (2)
Data updated Oct 16, 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 00380659982699), received between Jul 18, 2023 and Jul 18, 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 16, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 18, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
A HEALTHCARE PROFESSIONAL REPORTED THAT CAPSULOTOMY CENTER POSITION WAS PLACED WELL BELOW THE IRIS CENTER AND IRIS REPOSITIONING MANUALLY BROUGHT TO THE CENTER OF THE PUPIL AND WAS PLACED THERE IN THE UNKNOWN EYE OF A PATIENT, DURING CATARACT SURGERY. AFTER MANUALLY REPOSITIONING, THE SURGERY WAS COMPLETED WITHOUT PROBLEMS. THE PATIENT IDENTIFIER IS NOT AVAILABLE. THERE'S NO PATIENT HARM.
Patient problems: Insufficient Information
MAUDE report 17340637 ↗
Other Camera, Still, Microsurgical devices
- VERION™ 8065998270Alcon Laboratories, Inc. · Camera, Still, Microsurgical20 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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