The Recall Desk
SevereFDA (Devices)·Z-0989-2019·Announced 2019-03-13

Maquet Flat Screen Monitor Holder Recalled for Grounding Non-Compliance

Getinge US Sales LLC 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 criteria for a score of 4 (Severe) involving significant injury or property damage reports/risks.

Plain-English summary

Getinge US Sales LLC is recalling six units of the Maquet XS Flat Screen Monitor Holder, Configuration Part Number ARD268400150A. The affected units have serial numbers 500001 through 500006. These products are designed to support one or two medical-grade flat screens, either alone or in association with surgical lights.

The recall was initiated because the affected monitor holders might not be compliant with grounding requirements. This non-compliance 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 products were distributed to the US states of Arizona and Texas. The source text does not specify further instructions for consumers or healthcare facilities regarding the immediate handling of these units.

The recalled product

Product
Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A 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 500001 500002 500003 500004 500005 500006

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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