Home › MAQUET SAS › Maquet PowerLED II
Maquet PowerLED II
MAQUET SAS · Model ARDPWT229143A · UDI-DI 03700712406899
10
510(k) clearances
1,240
Adverse events (2 deaths)
49
Recalls
59
Facilities
Description
PWDII50SF VP AIM K4 16
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-06-04 | Baxter Healthcare Corporation | Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l |
| 2024-06-04 | Baxter Healthcare Corporation | Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2023-11-08 | Getinge Usa Sales Inc | A potential for a light system to fall in the operating room. |
| 2019-05-28 | Maquet Cardiovascular Us Sales, Llc | Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may r |
| 2019-05-28 | Maquet Cardiovascular Us Sales, Llc | Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may r |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.