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

Recall Z-0627-2013 — Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Kehler Strabe 31 Baden-Wuerttemberg 76437 Rastatt,Germany Used to support the lower extremities immediately before during and after surgery. The extension device is mounted to the YUNO operating table. The product may only be operated b

U.S. FDA — Device Enforcement · United States · 2012-11-02 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0627-2013
Date of alert: 2012-11-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Maquet Inc.
Product category: device
Product type: Devices

Reported risk: There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.

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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