Getinge recalls PowerLED/HLED and PowerLED300 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms.
A potential for a light system to fall in the operating room.
Getinge is recalling PowerLED/HLED and PowerLED300 OR Light Systems with specific model numbers because there is a risk of the light system falling in the operating room. This could lead to injury if the light falls on someone.
The light systems could fall in the operating room due to a design flaw that makes them unstable when in use. This poses a risk of injury if the light falls on a person.
Healthcare professionals using these light systems in operating rooms are most at risk. The recall applies to specific model numbers sold by Getinge.
Check the model numbers listed in the recall notice, which include EPS MB1, EPS MB3, and other specific codes. These light systems are used in operating rooms and were sold with the listed model numbers.
Look for the model numbers listed in the recall notice, such as EPS MB1, EPS MB3, and other specific codes.
The light system could fall in the operating room due to a design flaw that makes it unstable when in use.
Check the model numbers listed in the recall notice to see if your system is affected. If it is, you should contact Getinge for further instructions.
The recall states there is a potential for the light system to fall, which could lead to injury if it falls on someone. However, the remedy is not specified, so no immediate action is required beyond checking model numbers.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0763-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0763-2024 from Getinge. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.