Alcon Grieshaber Finesse MAXGrip REVOLUTION 706.13Recalls & reported problems
Alcon Laboratories, Inc. · GRIESHABER MAXGrip® REV DSP Forceps, 23G · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 07612717070707), received between Dec 13, 2021 and Jan 29, 2026 — classified as 1 injury, 14 malfunctions.
The most frequently reported specific device problem is “Difficult to Open or Close” (11 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 Close11
- Activation Problem2
- Adverse Event Without Identified Device or Use Problem1
- Fitting Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions13
- Insufficient Information1
- Macular Edema1
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 29, 2026Activation Problem
A CUSTOMER REPORTED THAT IN AN OPHTHALMIC FORCEPS TIPS DID NOT MEET. PROCEDURE DETAILS AND PATIENT IMPACT HAVE NOT BEEN PROVIDED. ADDITIONAL INFORMATION HAS BEEN REQUESTED; NONE HAS BEEN RECEIVED TILL DATE.
Patient problems: Insufficient Information
MAUDE report 24209053 ↗MalfunctionMar 26, 2025Activation Problem; Activation Problem
A CUSTOMER REPORTED THAT DURING VITRECTOMY SURGERY AN OPHTHALMIC FORCEPS WAS UNABLE TO OPEN. THE PROCEDURE WAS COMPLETED AFTER USING AN OPHTHALMIC SHARK SKIN. NO PATIENT HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21701994 ↗MalfunctionJan 22, 2025Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED THAT DURING VITREORETINAL SURGERY AN OPHTHALMIC FORCEPS DID NOT FUNCTIONED AS EXPECTED AND TIPS WOULD NOT MEET. THE PROCEDURE WAS COMPLETED WITH OTHER FORCEPS WITHOUT ANY PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21206103 ↗MalfunctionOct 14, 2024Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT DURING VITREORETINAL SURGERY, THE OPHTHALMIC FORCEPS WOULD NOT CLOSE COMPLETELY. THE SURGERY WAS COMPLETED BY USING ANOTHER FORCEPS. THERE WAS NO PATIENT IMPACT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20437811 ↗MalfunctionSep 23, 2024Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT AN OPHTHALMIC SURGICAL FORCEPS TIPS NOT STICKING/GRIPPING AT ALL DURING SURGERY IN THE LEFT EYE OF THE PATIENT. THE SURGERY WAS COMPLETED ON THE SAME DAY AFTER USING ANOTHER SHARK SKIN FORCEPS. THE TYPE OF PROCEDURE WAS NOT REPORTED. NO PATIENT IMPACT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20284964 ↗MalfunctionFeb 6, 2024Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT DURING A VIT-RET SURGERY, A FORCEPS EXHIBITED THE HANDLE DID NOT WORK PROPERLY. THE EXACT POSITION OF THE FORCEPS, WHETHER STICKING IN A FULL OPEN OR FULL CLOSED POSITION, REMAINS UNKNOWN. THE SURGERY WAS COMPLETED POST REPLACING THE PRODUCT. PATIENT IMPACT WERE NOT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18651901 ↗MalfunctionAug 14, 2023Difficult to Open or Close; Difficult to Open or Close
A HEALTHCARE PROFESSIONAL REPORTED THAT DURING A VIT RETINAL SURGERY AN OPHTHALMIC FORCEPS FAILED AS IT WAS NOT CLOSING PROPERLY. SURGERY WAS COMPLETED WITH AN ALTERNATE FORCEPS. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17539402 ↗MalfunctionAug 14, 2023Difficult to Open or Close; Difficult to Open or Close
A HEALTHCARE PROFESSIONAL REPORTED THAT DURING A VIT RETINAL SURGERY AN OPHTHALMIC FORCEPS FAILED AS IT WAS NOT CLOSING PROPERLY. SURGERY WAS COMPLETED WITH AN ALTERNATE FORCEPS. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17539390 ↗InjuryJun 15, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A INVESTIGATOR REPORTED IN A CLINICAL STUDY AFTER USING SURGICAL FORCEPS A MALE PATIENT EXPERIENCED WITH MACULAR EDEMA AFTER POST VITRECTOMY SURGERY. UNKNOW INTERVENTION WAS REPORTED AND THE SYMPTOMS WERE RESOLVED.
Patient problems: Macular Edema
MAUDE report 17134140 ↗MalfunctionJan 24, 2023Difficult to Open or Close; Difficult to Open or Close
A PHYSICIAN REPORTED THAT THE TIPS OF AN OPHTHALMIC FORCEPS DO NOT COME TOGETHER AND GRASP DURING SURGERY. THE SURGERY WAS COMPLETED AND THERE WAS NO REPORT OF ANY PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16233362 ↗MalfunctionJan 5, 2023Difficult to Open or Close; Difficult to Open or Close
A PHYSICIAN REPORTED THAT DURING A PROCEDURE AN OPHTHALMIC FORCEPS WERE NOT CLOSING AT THE TIPS. THE PROCEDURE WAS COMPLETED WITH ANOTHER FORCEPS USED. THERE WAS NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16102460 ↗MalfunctionAug 12, 2022Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT AN OPHTHALMIC FORCEPS DID NOT CLOSE DURING A SURGERY. THE SURGERY WAS COMPLETED SUCCESSFULLY BY REPLACING FORCEPS WITH ANOTHER ONE. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15217341 ↗MalfunctionAug 12, 2022Difficult to Open or Close; Difficult to Open or Close
A PHYSICIAN REPORTED THAT THE TIP OF AN OPHTHALMIC FORCEPS WAS UNABLE TO CLOSE PROPERLY DURING A SURGERY. THE SURGERY WAS COMPLETED SUCCESSFULLY BY REPLACING THE FORCEPS WITH ANOTHER ONE. THERE WAS NO REPORT OF ANY PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15217334 ↗MalfunctionApr 20, 2022Difficult to Open or Close; Difficult to Open or Close
A CUSTOMER REPORTED THAT THE OPHTHALMIC FORCEPS WOULD NOT CLOSE. PROCEDURE DETAILS AND PATIENT IMPACT WERE NOT REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NONE RECEIVE TILL DATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14161139 ↗MalfunctionDec 13, 2021Fitting Problem; Fitting Problem
AN OPHTHALMIC SURGEON REPORTED THAT AN OPHTHALMIC FORCEPS DID NOT OPEN AT THE END OF VERY FIRST GRAB. TROCARS ARE CONSISTENTLY TIGHT. ADDITIONAL INFORMATION HAS BEEN REQUESTED. ADDITIONAL INFORMATION RECEIVED CONFIRMED THAT THERE IS NO PROBLEM WITH THE TROCARS ONLY THAT THE FORCEPS DO NOT CLOSE PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12985124 ↗
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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