Iris Scissor SU-7-1055-11Recalls & reported problems
Elmed Instruments(Pvt)Ltd. · Intended Use: An iris scissors is used to complete the retinacular release as proximally as possible while the nerve is under vision and protected Packaging: Packaging shall be as per customer requirements e.g set of 25 or set of 50. · Class 1
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 G165SU71055110), received between Aug 1, 2025 and Aug 1, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Frayed” (2 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
- Material Frayed2
- Mechanical Jam2
Patient problems
- Discomfort2
- 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.
MalfunctionAug 1, 2025Material Frayed; Mechanical Jam; Material Frayed; Mechanical Jam
MalfunctionAug 1, 2025Material Frayed; Mechanical Jam; Material Frayed; Mechanical Jam
Other Scissors, Ophthalmic devices
- Handle Assy, Single-Use, Packaged DFH-1028Microsurgical Technology, Inc. · Scissors, Ophthalmic1 recall0 reports
- Sklar Instruments 96-2541Sklar Corporation · SCISSORS, OPHTHALMIC1 recall0 reports
- Sklar Instruments 96-2542Sklar Corporation · SCISSORS, OPHTHALMIC1 recall0 reports
- Alcon Grieshaber REVOLUTION 25+ 705.52PAlcon Laboratories, Inc. · SCISSORS, OPHTHALMIC28 reports
- Alcon Grieshaber REVOLUTION 706.52Alcon Laboratories, Inc. · SCISSORS, OPHTHALMIC19 reports
- Alcon Grieshaber REVOLUTION 705.52Alcon Laboratories, Inc. · SCISSORS, OPHTHALMIC13 reports
- Alcon Grieshaber 25+ 725.52PAlcon Laboratories, Inc. · SCISSORS, OPHTHALMIC10 reports
- Alcon Grieshaber 723.52Alcon Laboratories, Inc. · SCISSORS, OPHTHALMIC6 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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