Maquet recalls Brainlab camera light systems with specific model numbers due to potential for falling in operating rooms. Affected units include BRAINLAB CAMERA - ARDEQT269000A and other variants.
A potential for a light system to fall in the operating room.
Maquet is recalling specific Brainlab camera light systems that could fall in operating rooms. This hazard poses a risk of injury to surgical staff or patients if the light system falls during use.
The light system could fall from its mounting in the operating room, potentially causing injury to staff or patients. This risk occurs during normal surgical procedures when the light is in use.
Healthcare professionals using these light systems in operating rooms are most at risk. Patients and staff in surgical settings may be affected if the light falls during procedures.
Check for model numbers listed in the recall: BRAINLAB CAMERA - ARDEQT269000A, BRAINLAB CAMERA - ARDEQT269000C, and other variants. These units were sold with specific UDI-DI codes.
Look for the model numbers listed in the recall, such as BRAINLAB CAMERA - ARDEQT269000A or similar variants.
Reach out to Getinge Usa Sales Inc for further assistance or to confirm if your unit is affected.
The recall is due to a potential for the light system to fall in the operating room, which could cause injury to staff or patients.
Check for the specific model numbers listed in the recall, such as BRAINLAB CAMERA - ARDEQT269000A or other variants with matching UDI-DI codes.
Contact Getinge Usa Sales Inc to confirm if your unit is affected and follow their instructions.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-0761-2024 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-0761-2024 from Maquet. 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.
