LUCEA LED® ARDLCA506006ARecalls & reported problems
Maquet Sas · LCA100 MOBILE UPGRADE · Class 2
All models of LUCEA LED (33)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Nov 8, 2023Open, Classified
A potential for a light system to fall in the operating room.
Z-0759-2024 · Root cause: Equipment maintenance · Recall details · FDA record ↗
Other Led light source devices
- VIDEO SYSTEM CENTER CV-170Olympus Medical Systems Corp. · Led Light Source811 reports
- SpyGlass DS M00546650Boston Scientific Corporation · Led light source154 reports
- LUCEA LED® ARDLCA209016AMaquet Sas · Led light source1 recall0 reports
- LUCEA LED® ARDLCA506000AMaquet Sas · Led light source1 recall0 reports
- LUCEA LED® ARDLCA109008AMaquet Sas · Led light source1 recall0 reports
- Olympus WA91502AOLYMPUS Winter & Ibe GmbH · Led Light Source29 reports
- n.a. TL300Karl Storz GmbH & Co. KG · Led light source11 reports
- VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500Olympus Medical Systems Corp. · Led Light Source9 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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