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LUCEA LED® ARDLCA309008ARecalls & reported problems

Maquet Sas · LCA 10 MOBILE · Class 1

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

  1. 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

All Device, Medical Examination, Ac Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.