FDAClass IIRecall started August 7, 2026

PowerLED 300 Concealed Lighting System Recall

PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;

Why was PowerLED 300 Concealed Lighting System recalled?

The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

The official FDA identifier list is too long to reproduce here. Compare your item with the complete list in the agency notice.

Which lot codes, UPCs or models are affected?

The official FDA record has an unusually long identifier list. Check the complete lot, serial and model numbers in the linked agency notice.

Open the complete official FDA record

Product
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;
Recalling firm
Maquet SAS
Quantity
667
Distribution
US Nationwide distribution.
Recall started
August 7, 2026
Report date
September 30, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls