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Maquet PowerLED II

MAQUET SAS · Model ARDPWT239040A · UDI-DI 03700712409166

FTD
10
510(k) clearances
1,238
Adverse events (2 deaths)
49
Recalls
59
Facilities

Description

PWDII70SF AIM CL MHS013 K4 1116

Recalls

DateFirmReason
2024-06-04Baxter Healthcare CorporationBaxter 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
2024-06-04Baxter Healthcare CorporationBaxter 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
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2023-11-08Getinge Usa Sales IncA potential for a light system to fall in the operating room.
2019-05-28Maquet Cardiovascular Us Sales, LlcPotential 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 re
2019-05-28Maquet Cardiovascular Us Sales, LlcPotential 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 re

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Data 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.