Laser Probe, straight, with DORC connector 20 gauge / 0.9mm 7011.DORCRecalls & reported problems
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Class 2
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 08717872013992), received between Apr 6, 2018 and Apr 6, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Operational Issue” (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
- Device Operational Issue1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2018Device Operational Issue; Device Operational Issue
(B)(6) HAS REPORTED : THE LASER PROBE WAS DEFECT. IT LOOKED LIKE THE CABLE IS BROKEN BECAUSE THE LASER SHOT COMES OUT IN THE OR. ALL EMPLOYEES ANGRY ABOUT THIS. SAMPLE IS AVAILABLE. NO INJURY WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7402684 ↗
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- Directional Laser Probe with Alcon / Lumenis connector.(27 gauge / 0.4 mm) 7227.ALCD.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Laser, Ophthalmic1 recall0 reports
- EVA, combined machine including Laser (DORC connector) 8000.COM02D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Laser, Ophthalmic44 reports
- EVA, combined machine including Laser (SMA connector) 8000.COM03D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Laser, Ophthalmic20 reports
- Alcon, Engauge 8065751709Alcon Laboratories, Inc. · Laser, ophthalmic14 reports
- Alcon, Engauge 8065750991Alcon Laboratories, Inc. · Laser, ophthalmic10 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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