Alcon Greishaber Finesse 338.23Recalls & reported problems
Alcon Laboratories, Inc. · 23G FINESSE® Flex Loop DSP · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07612717071421), received between Aug 15, 2025 and Aug 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionAug 15, 2025Break; Break
A CUSTOMER REPORTED THAT DURING SURGERY THE HANDLE OF AN OPHTHALMIC SCRAPPER CAME LOOSE FROM THE CABLE AND PLUNGED INTO THE PATIENT'S RETINA. THE PROCEDURE AND PATIENT DETAIL WERE NOT REPORTED. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: Insufficient Information
MAUDE report 22813350 ↗
Other Hook, ophthalmic devices
- Sklar Instruments 96-2224ASklar Corporation · Hook, ophthalmic1 recall0 reports
- miLOOP 303071-9090-000Carl Zeiss Meditec AG · Hook, Ophthalmic1 recall0 reports
- Alcon Grieshaber 25+ Finesse 338.25PAlcon Laboratories, Inc. · Hook, ophthalmic21 reports
- Alcon Grieshaber 27+ Finesse 338.27Alcon Laboratories, Inc. · Hook, ophthalmic11 reports
- Alcon Grieshaber 337.92Alcon Laboratories, Inc. · Hook, ophthalmic2 reports
- Millennium 92-H0499Avalign Technologies, Inc. · Hook, ophthalmic1 report
- Osher/Malyugin Ring Manipulator MAL-0003Microsurgical Technology, Inc. · Hook, Ophthalmic1 report
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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