Maquet PowerLED 300 Concealed Lighting System
The PowerLED 300 Concealed Lighting System can detach at the junction between the spring arm and suspension arm and fall, causing potential injury.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Maquet SAS is recalling the PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) because the device can detach at the junction between the spring arm and suspension arm and fall, causing potential injury. The recall began August 7, 2026, and was added to the FDA's Enforcement Report on September 18, 2026. The product was distributed nationwide in the US.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number is listed.
PowerLED 300 Concealed Lighting System
- Model
- ARD568474114A
- ARD567501286
Details
- Company began the recall
- Sold in
US Nationwide distribution.
- Event ID
- 99696
- Recall No.
- Z-3224-2026
- Company
- Maquet SASOrleans Cedex 2, France
- Hazard
- Device defect
- Recall type
- Voluntary: Firm initiated
- Customers told by
- Letter
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
