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FDAFDA · Food and drugs·Recall number Z-0764-2024

Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD567505961C, AXL 5002 - ARD567501962C, AXL 5002S - ARD567505962C, AXL 5501 - ARD567501960A, AXL 5501 - ARD567501960C, AXL 5501S - ARD567505960C, AXL+5001 DF - ARD567502961C, AXL+5001 SF - ARD567502861C, AXL+5301 DF - ARD567502971C, AXL+5501 DF - ARD567502960C, AXL+5501 SF - ARD567502860C, AXL+5531 DF - ARD567502930C, AXL50 RLC - ARDRLC309000C, AXL50 RLC - ARDRLC309006C, AXL5003 - ARD567505968C, AXL5003 US - ARD567505969C

Published January 24, 2024 · Recall initiated: November 8, 2023

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

A potential for a light system to fall in the operating room.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Getinge Usa Sales Inc
Distributor
US Nationwide. Global Distribution.
Lot
All systems affected
Risk classification
Class II
Area (FDA)
device
Country
United States

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