Drug recall
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1…
FDA recall event 99696 · Class II · Maquet SAS
Key facts
| Event ID | 99696 |
|---|---|
| Recall numbers | Z-3224-2026 |
| Recalling firm | Maquet SAS |
| Product type | Devices |
| Products | PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2. ARD567501286; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Aug 7, 2026 |
| Report date | Sep 30, 2026 |
| City | Orleans Cedex 2 |
| Country | France |
| FEI number | 3002465150 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: