Alcon 00380650002525Recalls & reported problems
Alcon Laboratories, Inc. · 27GA Chandelier · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Aug 5, 2025Open, Classified
Due to incomplete seals in the pouch which provide the sterile barrier.
Z-0307-2026 · Root cause: Process control · FDA record ↗
Other Endoilluminator devices
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- Synergetics 56.34.25PSynergetics USA, Inc. · Endoilluminator2 reports
- Disposable Eckardt Twinlight Chandelier. (27 gauge / 0.4mm) 3269.MBD27D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · Endoilluminator1 report
- Synergetics 56.21.25PSSynergetics USA, Inc. · Endoilluminator1 report
- Synergetics 56.54.27PSynergetics USA, Inc. · Endoilluminator1 report
- Shielded TotalView Endoillumination Probe incl illuminated scleral depressor 25G 3269.SBS05D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · 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
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.