Synergetics 56.54.27PRecalls & reported problems
Synergetics USA, Inc. · 27ga Oshima Vivid Chandelier · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20841305107506), received between Mar 6, 2023 and Mar 6, 2023 — classified as 1 injury.
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
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 6, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE USER FACILITY IN JAPAN REPORTED AFTER SURGERY, THE TIP OF THE PROBE BECAME CURLED SOLID, AND COULD NOT BE PULLED OUT OF THE INCISION. AN INCISION WAS REQUIRED TO PULL THE PROBE OUT OF THE PATIENTS EYE. NO HEALTH PROBLEMS WERE OBSERVED IN THE PATIENT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 16490752 ↗
Other Endoilluminator devices
- Alcon 00380650002525Alcon Laboratories, Inc. · Endoilluminator1 recall0 reports
- Alcon 00380650002532Alcon Laboratories, Inc. · Endoilluminator1 recall0 reports
- Synergetics 56.34.25PSynergetics USA, Inc. · Endoilluminator2 reports
- Shielded TotalView Endoillumination Probe incl illuminated scleral depressor 25G 3269.SBS05D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Endoilluminator1 report
- Synergetics 56.21.25PSSynergetics USA, Inc. · Endoilluminator1 report
- Shielded TotalView Endoillumination Probe incl illuminated scleral depressor 23G 3269.SBS06D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Endoilluminator1 report
- Disposable Eckardt Twinlight Chandelier. (27 gauge / 0.4mm) 3269.MBD27D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Endoilluminator1 report
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