LUCEA LED® ARDLCA309009ARecalls & reported problems
Maquet Sas · LCA 40 MOBILE · Class 1
Data updated Oct 13, 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. How this data works · Data updated Oct 13, 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 · FDA record ↗
Other Device, Medical Examination, Ac Powered devices
- Chromophare CH00000001Berchtold Holding GmbH · DEVICE, MEDICAL EXAMINATION, AC POWERED3 recalls50 reports
- LUCEA LED® ARDLCA109006AMaquet Sas · Device, Medical Examination, Ac Powered1 recall0 reports
- LUCEA LED® ARDLCA309008AMaquet Sas · Device, Medical Examination, Ac Powered1 recall0 reports
- LUCEA LED® ARDLCA209021AMaquet Sas · Device, Medical Examination, Ac Powered1 recall0 reports
- Hillrom™ 4058110Baxter Medical Systems GmbH + Co. KG · Device, medical examination, ac powered4 reports
- HexaLux HexaLux Ceiling MountSteris Corporation · Device, medical examination, ac powered4 reports
- HexaLux HexaLux Ceiling MountSteris · Device, medical examination, ac powered4 reports
- Chromophare F300 CE2863075Berchtold Holding GmbH · DEVICE, MEDICAL EXAMINATION, AC POWERED2 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 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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