Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Maquet Axcel / Axcel + OR Light Systems Recalled by Getinge Usa Sales Inc Due to A potential for a light system to fall...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Getinge Usa Sales Inc directly.
Affected Products
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
Quantity: 236793 units in total
Why Was This Recalled?
A potential for a light system to fall in the operating room.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Getinge Usa Sales Inc
Getinge Usa Sales Inc has 48 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report