Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top Recalled by Maquet Medical Systems, Usa Due to As a result of a small number of...
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 Maquet Medical Systems, Usa directly.
Affected Products
Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top Version 1180.16 The carbon-fibre MAGNUS table top (1180-16XX) serves to support and position patients for surgical procedures (e.g. cardiovascular surgery) and interventional examination immediately before, during and after the surgical phase. The table top is radiotranslucent and enables intraoperative use of X-ray equipment.
Quantity: 164 Units located in 27 Countries
Why Was This Recalled?
As a result of a small number of customer complaints, MAQUET conducted an investigation and identified a potential problem with specific MAGNUS Carbon-Fibre Table Tops manufactured between February 23, 2010 and February 28, 2012 and distributed between November 11, 2010 and April 6, 2012. There is a potential issue with the motor brakes for the longitudinal shift drive, and the tilt drive.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Medical Systems, Usa
Maquet Medical Systems, Usa has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report