Alcon Grieshaber REVOLUTION 706.44Recalls & reported problems
Alcon Laboratories, Inc. · REVOLUTION DSP 23G ILM Forceps · Class 1
All models of Alcon Grieshaber REVOLUTION (13)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 07612717066960), received between Aug 18, 2021 and Feb 27, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Difficult to Open or Close” (8 reports).
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
- Difficult to Open or Close8
- Break3
- Activation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
- Insufficient Information4
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2026Break
A CUSTOMER REPORTED THAT DURING SURGERY AN OPHTHALMIC FORCEPS THAT HAD A PIECE OF A PRODUCT THAT CAME OFF. PROCEDURE DETAILS AND PATIENT IMPACT WERE NOT REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT IS NOT AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Insufficient Information
MAUDE report 24470667 ↗MalfunctionFeb 27, 2026Break
A CUSTOMER REPORTED THAT DURING SURGERY FOR AN OPHTHALMIC FORCEPS HAD A PIECE THAT CAME OFF WITH NO PROPER GRIPPING. DETAILS RELATED TO PATIENT HARM HAVE NOT BEEN REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT IS NOT AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Insufficient Information
MAUDE report 24469322 ↗MalfunctionNov 7, 2025Break; Break
THE GOVERNMENT AGENCY REPORTED THAT OPHTHALMIC FORCEPS TIP FRACTURED DURING USE. THERE WAS NO PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23495472 ↗MalfunctionApr 28, 2025Activation Problem; Activation Problem
A PHYSICIAN REPORTED THAT DURING VITRECTOMY SURGERY WHEN USING FOR MEMBRANE STRIPPING, THE TIP OF THE OPHTHALMIC FORCEPS CANNOT BE OPENED WHEN PRESSING THE HANDLE. THE SURGERY WAS COMPLETED ON THE SAME DAY WITH ALTERNATIVE FORCEPS AND THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21916851 ↗MalfunctionAug 9, 2024Difficult to Open or Close; Difficult to Open or Close
ADDITIONAL INFORMATION HAS BEEN RECEIVED AND REPORTED THAT THE SURGERY WAS COMPLETED ON THE SAME DAY AFTER REPLACING WITH ANOTHER FORCEPS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19946626 ↗MalfunctionAug 8, 2024Difficult to Open or Close; Difficult to Open or Close
A HEALTHCARE PROFESSIONAL REPORTED THAT JAWS OF AN OPHTHALMIC SURGICAL FORCEPS DO NOT OPEN PROPERLY FOR USE DURING SURGERY. THE SURGERY WAS COMPLETED ON THE SAME DAY AFTER REPLACING WITH ANOTHER NEW FORCEPS. NO PATIENT IMPACT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19944032 ↗MalfunctionApr 23, 2024Difficult to Open or Close; Difficult to Open or Close
A NURSE REPORTED THAT AN OPHTHALMIC FORCEPS HEAD CLAMP ARM COULD NOT BE CLOSED DURING VITRECTOMY SURGERY. THE SURGERY WAS COMPLETED ON THE SAME DAY. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19162484 ↗MalfunctionApr 10, 2024Difficult to Open or Close; Difficult to Open or Close
ADDITIONAL INFORMATION RECEIVED CLARIFYING THAT THE TIP OF THE FORCEPS WAS BENT.
Patient problems: Insufficient Information
MAUDE report 19077900 ↗MalfunctionApr 1, 2024Difficult to Open or Close; Difficult to Open or Close
A NURSE REPORTED THAT AN FORCEP HEAD CLAMP ARM NOT BE CLOSED DURING OPEN POSITION DURING VITRECTOMY SURGERY. THE SURGERY WAS COMPLETED ON THE SAME DAY. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19010928 ↗MalfunctionFeb 22, 2024Difficult to Open or Close; Difficult to Open or Close
A NURSE REPORTED THAT DURING A VITRECTOMY SURGERY AN OPHTHALMIC FORCEPS WAS NOT OPENING AND CLOSING. SURGERY WAS COMPLETED WITH AN ALTERNATIVE FORCEPS WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18756944 ↗MalfunctionJan 17, 2024Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT AN OPHTHALMIC FORCEPS DID NOT OPEN. PROCEDURE DETAILS AND PATIENT IMPACT WERE NOT REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NONE RECEIVED TILL DATE.
Patient problems: Insufficient Information
MAUDE report 18524598 ↗MalfunctionAug 18, 2021Difficult to Open or Close; Difficult to Open or Close
A PHYSICIAN REPORTED THAT MULTIPLE FORCEPS FAILED TO ACTUATE PROPERLY DURING SEPARATE VITRECTOMY PROCEDURES. ANOTHER FORCEPS WAS OPENED IN EACH EVENT AND THE SURGERY WAS COMPLETED. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12335536 ↗
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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