[Recalled] 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
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | 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 |
|---|---|
| Brand / manufacturer | Maquet Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0627-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 02 November 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Maquet Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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