Getinge recalls specific Maquet Prismalix OR light systems due to potential for falling in operating rooms. Affected models include 3001, 4001, 6001K, and others with catalog numbers starting with ARD567. No remedy is stated in the recall notice.
A potential for a light system to fall in the operating room.
Getinge is recalling specific Maquet Prismalix OR light systems that could fall in operating rooms. This hazard poses a risk of injury to healthcare workers during surgery. Affected units have model numbers and catalog numbers listed in the recall notice.
The light systems could fall from their mounting in the operating room due to a design flaw. This might cause injury to healthcare workers or patients if the light falls during surgery.
Healthcare professionals using the recalled Maquet Prismalix OR light systems in operating rooms are most at risk. Patients and staff could be injured if the light system falls during surgery.
Check for model numbers starting with 3001, 4001, 6001K, or 8401, along with catalog numbers beginning with ARD567. The recall includes specific combinations like 3001 - ARD567424001C and 4001 S/DF - ARD567211211C.
Identify your Maquet Prismalix OR light system's model number and catalog number to confirm if it's affected by this recall.
The recall is due to a potential risk of the light system falling in the operating room, which could cause injury to healthcare workers or patients.
Affected models include 3001, 4001, 6001K, and others with specific catalog numbers starting with ARD567, such as 3001 - ARD567424001C and 4001 S/DF - ARD567211211C.
The recall notice does not specify any remedy or action for affected units.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0767-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0767-2024 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.
