Alcon Grieshaber 723.44Recalls & reported problems
Alcon Laboratories, Inc. · Advanced DSP Tip ILM Forceps, 23G · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07612717070936), received between Jun 27, 2023 and Aug 15, 2025 — classified as 1 injury, 1 malfunction.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Fitting Problem1
Patient problems
- Insufficient Information1
- Laceration(s)1
- Retinal Detachment1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 15, 2025Fitting Problem; Fitting Problem
A PHYSICIAN REPORTED THAT WHILE INSERTING FORCEPS INTO A TROCAR BEFORE SURGERY IT WAS TIGHTLY LODGED AND COULD NOT BE REMOVED. PROCEDURE WAS COMPLETED. PATIENT HARM WAS NOT REPORTED.
Patient problems: Insufficient Information
MAUDE report 22813979 ↗InjuryJun 27, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A CUSTOMER REPORTED VIA A CLINICAL STUDY THAT DURING A VITRECTOMY SURGERY WHILE USING AN OPHTHALMIC DISPOSABLE PRODUCT A PATIENT EXPERIENCED RETINAL SURFACE DAMAGE AND LACERATION. NO FURTHER INFORMATION EXPECTED AS THE DETAILS WERE RECEIVED FROM A CLINICAL STUDY.
Patient problems: Laceration(s); Retinal Detachment
MAUDE report 17210917 ↗
Other Forceps, ophthalmic devices
- Vortex Surgical Inc VS0740.25Vortex Surgical, Inc. · Forceps, Ophthalmic2 recalls0 reports
- 25ga DEX Stiff Maculorhexis Forceps DVF4019-25-SKatalyst Surgical LLC · Forceps, Ophthalmic2 recalls0 reports
- Alcon Grieshaber REVOLUTION 25+ 705.44PAlcon Laboratories, Inc. · Forceps, ophthalmic93 reports
- 27ga DEX™ Yoneda Super Grip Forceps DVF4036-27Katalyst Surgical LLC · Forceps, Ophthalmic1 recall4 reports
- 25ga DEX Stiff End Grasper Forceps DVF4022-25-SKatalyst Surgical LLC · Forceps, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0740.23Vortex Surgical, Inc. · Forceps, Ophthalmic1 recall0 reports
- Vortex Surgical Inc VS0744.25Vortex Surgical, Inc. · Forceps, Ophthalmic1 recall0 reports
- Vortex Surgical Inc. VS0751.25Vortex Surgical, Inc. · Forceps, Ophthalmic1 recall0 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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