Alcon Grieshaber 337.92Recalls & reported problems
Alcon Laboratories, Inc. · GRIESHABER™ 45° Pic DSP 25G · Class 1
All models of Alcon Grieshaber (17)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07612717068346), received between Apr 14, 2022 and Sep 8, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fitting Problem” (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
- Appropriate Device Problem Term/Code Not Available1
- Fitting Problem1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
A PHARMACIST REPORTED THAT DURING A SURGERY, AN OPHTHALMIC PROBE STOPPED WORKING. THE PROCEDURE DETAILS AND PATIENT IMPACT HAVE NOT BEEN PROVIDED. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NONE RECEIVED TILL DATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15377774 ↗MalfunctionApr 14, 2022Fitting Problem; Material Twisted/Bent; Fitting Problem; Material Twisted/Bent
A HEALTHCARE PROFESSIONAL REPORTED THAT DURING A VITRECTOMY PROCEDURE AN OPHTHALMIC TIP WAS BENT AND IT COULD NOT GO THROUGH THE TROCAR. PATIENT IMPACT WAS NOT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14110721 ↗
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
- Millennium 92-H0499Avalign Technologies, Inc. · Hook, ophthalmic1 report
- Osher/Malyugin Ring Manipulator MAL-0003Microsurgical Technology, Inc. · Hook, Ophthalmic1 report
- Alcon Greishaber Finesse 338.23Alcon Laboratories, 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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