FDA · Medical devices ·
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers recall
Maquet SAS recalled PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers on September 30, 2026 because of the potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury. It was sold nationwide.
Why it was recalled
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.
What's recalled
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286;
Quantity: 667
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Maquet SAS, Orleans Cedex 2
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution. - Status
- Ongoing
- Recall number
- Z-3224-2026
- Source
- U.S. Food and Drug Administration
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