GETINGE recalls Maquet flat screen monitor holders with specific part numbers due to potential electric shock risk from improper grounding. Affected units may cause mild to fatal shocks when used with 100-220V power.
The affected flat screen monitor holders might not be compliant with grounding requirements. As a consequence, there is a risk of mild to severe/fatal electric shock under certain conditions while using the flat screen monitor holder with voltage of 100-220V.
GETINGE is recalling Maquet flat screen monitor holders that might not meet grounding safety standards. This could lead to electric shock ranging from mild to fatal if used with standard household voltage.
The monitor holders might not properly ground electrical current, creating a path for electric shock. This risk increases when the holder is used with standard 100-220V power sources, potentially causing injury or death.
Healthcare professionals using the monitor holders in medical settings are most at risk. Patients and staff near the monitor could be affected if the holder becomes energized.
Check for the part number ARD268400140A on the monitor holder. The product is designed for medical use with flat screens and surgical lights. Serial numbers are listed on the product.
Look for the part number ARD268400140A or serial numbers on the monitor holder.
Yes, the monitor holders might cause mild to fatal electric shock if not properly grounded, especially when used with standard household voltage.
Check for the part number ARD268400140A or serial numbers on the monitor holder. The product is designed for medical use with flat screens and surgical lights.
The recall record does not specify a remedy, so contact GETINGE US SALES LLC for further instructions.
We’ve drafted a message you can send GETINGE to request your refund or repair — edit it as you like.
Subject: Recall Z-0988-2019 — GETINGE GETINGE Hello, I own a GETINGE that is covered by recall Z-0988-2019 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.
