The Recall Desk
SevereFDA (Devices)·Z-0987-2019·Announced 2019-03-13

Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

Getinge is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The source text explicitly states a risk of 'severe/fatal electric shock,' which aligns with the rubric criterion for 'significant injury/property-damage reports' or high-risk hazards warranting a Severe classification.

Plain-English summary

Getinge US Sales LLC is recalling six units of the Maquet XS Flat Screen Monitor Holder, model XS32 SPE, Configuration Part Number ARD22201040A. The affected units are identified by serial numbers 500009 through 500014. These products were distributed to facilities in Arizona and Texas.

The recall is being issued because the monitor holders might not be compliant with grounding requirements. This defect creates a risk of mild to severe or fatal electric shock under certain conditions when the holder is used with a voltage of 100-220V. The product is designed to support one or two medical-grade flat screens, either alone or in association with surgical lights.

Healthcare facilities that have received these specific serial numbers should stop using the affected monitor holders and contact Getinge US Sales LLC for instructions on how to resolve the issue.

The recalled product

Product
Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
Manufacturer
GETINGE US SALES LLC
Category
Medical Device — Surgical Equipment
Hazard
Affected units
6

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Serial Numbers 500009 500010 500011 500012 500013 500014

Distribution

Distributed in 2 states:

Part of a larger recall action

This product is one of 4 recalled by GETINGE US SALES LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 4 products in this recall →

Related recalls

Same manufacturer · GETINGE US SALES LLC

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Same hazard · electric shock

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