Class II
Medical Device Recall: Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.
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-0771-2024
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.