Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2108-2012 — 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

U.S. FDA — Device Enforcement · United States · 2012-04-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2108-2012
Date of alert: 2012-04-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Maquet Medical Systems, Usa
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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