Maquet SAS recalls PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2.
Maquet recalls PowerLED 300 Concealed Lighting Systems with specific model numbers due to potential detachment at spring arm junction causing injury. Affected units include serial numbers listed in the recall notice.
Use caution until it’s fixed
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.
What happened, in plain English
Maquet is recalling PowerLED 300 Concealed Lighting Systems with specific model numbers because the device can detach at the spring arm and suspension arm junction, potentially causing injury. Owners should check if their unit has the listed model numbers or serial numbers. Read more at govinfonow.com/recall/1292645-maquet-powerled-300-concealed-lighting-system-recall-risk-of-detachment.
Source Summary by GovInfoNow · govinfonow.com/recall/1292645-maquet-powerled-300-concealed-lighting-system-recall-risk-of-detachment · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3224-2026
Cite this page
“Maquet PowerLED 300 Concealed Lighting System Recall: Risk of Detachment and Injury.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292645-maquet-powerled-300-concealed-lighting-system-recall-risk-of-detachment. Based on FDA recall #Z-3224-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3224-2026%22&limit=1).
Why it’s dangerous
The device can detach at the junction between the spring arm and suspension arm, causing it to fall and potentially injure someone nearby. This risk occurs when the connection between these parts becomes loose or fails under normal use conditions.
Who’s affected
Owners of PowerLED 300 Concealed Lighting Systems with model numbers ARD568474114A or ARD567501286 and the listed serial numbers are affected. Those using the system in areas where it could detach and fall are at higher risk.
How to tell if you have this one
Check if your PowerLED 300 Concealed Lighting System has model numbers ARD568474114A or ARD567501286. The serial numbers listed in the recall notice (over 100 numbers) are also affected.
- Brand
Maquet- Category
Medical device
What to do — step by step
Check Model Numbers
Look for model numbers ARD568474114A or ARD567501286 on the device.
Verify Serial Numbers
Confirm if your unit's serial number matches any of the listed serial numbers in the recall notice.
Questions people ask
What is the hazard with the PowerLED 300 Concealed Lighting System?
The device can detach at the junction between the spring arm and suspension arm, potentially causing injury if it falls.
How can I check if my PowerLED 300 is affected?
Check if your model number is ARD568474114A or ARD567501286, and verify your serial number against the list of over 100 numbers provided in the recall notice.
Do I need to stop using the PowerLED 300 immediately?
No, but you should check if your unit is affected and take action if it is. The recall does not require immediate discontinuation of use.
Contact Maquet
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-3224-2026 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-3224-2026 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3224-2026 (August 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3224-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.