GETINGE recalls Maquet XS Flat Screen Monitor Holders with serial numbers 500009-500014 due to potential electric shock risk from improper grounding. Affected units may cause mild to severe electric shock 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 specific Maquet XS Flat Screen Monitor Holders that might not be properly grounded. This could cause mild to severe electric shock, including fatal shock, when used with standard electrical outlets.
The monitor holders might not meet grounding requirements, meaning electricity could flow through the device to a person during use. This risk is highest when the device is connected to standard 100-220V electrical outlets.
Medical facilities using the recalled monitor holders with serial numbers 500009 through 500014 are most at risk. Healthcare workers and patients using these devices could face electric shock.
Check for serial numbers 500009 through 500014 on the monitor holder. The product is designed for medical use with flat screens and surgical lights.
Immediately stop using the monitor holder if it has a serial number between 500009 and 500014.
The affected monitor holders might not be compliant with grounding requirements, which could lead to electric shock when used with standard electrical outlets.
The Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A with serial numbers 500009 through 500014.
Look for serial numbers 500009 through 500014 on the monitor holder. The product is designed for medical use with flat screens and surgical lights.
We’ve drafted a message you can send GETINGE to request your refund or repair — edit it as you like.
Subject: Recall Z-0987-2019 — GETINGE GETINGE Hello, I own a GETINGE that is covered by recall Z-0987-2019 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.
