Recall database

Light Based Device For Dry Age-Related Macular Degeneration recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–1 of 1 recalls

Class IIIOngoingZ-2046-2025

U.S. customers were shipped devices that were configured for the European Union and were unable to plug the device in the electrical outlet.

LUMITHERA INCWAJul 9, 2025