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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 1 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 3 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 2 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 1 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 2 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

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

All Forceps, ophthalmic devices →

Sources and updates

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