Class II

Medical Device Recall: Maquet G8 / G8E OR Light Systems, Model Numbers and Catalog Numbers G8 LC E - ARD568131211C, G8G8 DF E - ARD568121111C, G8G8FS DF - ARD568121131C

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-0769-2024

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.