Getinge recalls specific OR light systems due to potential for falling in operating rooms. Affected models include XTen and X10 series with listed catalog numbers. Consumers should check their product details to determine if recalled.
A potential for a light system to fall in the operating room.
Getinge is recalling certain operating room light systems that could fall in the operating room. This hazard poses a risk of injury to healthcare workers during surgery.
The light systems could fall during use in the operating room, potentially causing injury to staff or patients. This risk occurs because the systems are not securely anchored in the surgical environment.
Healthcare professionals using the recalled light systems in operating rooms are most at risk. Patients and staff in surgical settings may be affected if the light system falls.
Check for the following model numbers and catalog numbers: XTen OR Light Systems with catalog numbers like 3001 HMD14 - ARD567732001C, X TEN DUO - ARD568221510C, and other listed variants. These products were sold by Getinge in the U.S. market.
Identify your light system's model and catalog number to see if it matches the recalled items listed in the notice.
The recall indicates a potential risk of falling in the operating room, so they should not be used until the remedy is applied. The manufacturer has not provided a specific fix yet.
Look for the model numbers and catalog numbers listed in the recall notice, such as XTen OR Light Systems with catalog numbers like 3001 HMD14 - ARD567732001C or X TEN DUO - ARD568221510C.
The recall does not specify a remedy, so contact Getinge directly to determine next steps for affected products.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0766-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0766-2024 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.
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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.
