27ga DEX™ Morris ILM Forceps DVF4033-27Recalls & reported problems
Katalyst Surgical LLC · 27ga DEX™ Morris ILM Forceps · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10817489025434), received between Aug 12, 2026 and Aug 12, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Device Damaged Prior to Receipt by User1
- Difficult to Open or Close1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 12, 2026Device Damaged Prior to Receipt by User
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50229733 ↗MalfunctionAug 12, 2026Difficult to Open or Close
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50229732 ↗MalfunctionAug 12, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50229730 ↗
Other Probe, Trabeculotomy devices
- 27ga DEX™ Super Grip Forceps DVF4034-27Katalyst Surgical LLC · Probe, Trabeculotomy1 recall2 reports
- 25ga DEX™ Super Grip Forceps DVF4034-25Katalyst Surgical LLC · Probe, Trabeculotomy1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page