Class II

Medical Device Recall: Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C

Getinge Usa Sales Inc · November 8, 2023

Reason for Recall

A potential for a light system to fall in the operating room.

Distribution

US Nationwide. Global Distribution.

States Affected

NATIONWIDE

Quantity Affected

236793 units in total

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0765-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.