Engauge, Vektor 8065752554Recalls & reported problems
Alcon Laboratories, Inc. · 23GA ARTICULATING ILLUMINATED LASER PROBE · Class 2
All models of Engauge, Vektor (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00380657525546), received between Jun 13, 2022 and Jun 13, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Component” (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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Defective Component1
- Fitting Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 13, 2022Fitting Problem; Defective Component; Appropriate Device Problem Term/Code Not Available; Fitting Problem; Defective Component; Appropriate Device Problem Term/Code Not Available
A PHYSICIAN REPORTED THAT DURING A SURGERY AN OPHTHALMIC LASER PROBE WAS STUCK, THE TIP WAS FOUND DAMAGED AND THE LIGHT BEAM WAS NOT FOCUSING CORRECTLY. PROCEDURE WAS COMPLETED BY REPLACING THE PRODUCT. THERE WAS NO PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14679253 ↗
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- Infiniti 8065752160Alcon Laboratories, Inc. · Instrument, vitreous aspiration and cutting, ac-powered54 reports
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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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