Class II
Medical Device Recall: PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;
Maquet SAS · August 7, 2026
Reason for Recall
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
667
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3224-2026
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.