FDA Device 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…
- FDA Device
- Class II
- terminated
- Published 2013-01-09
On 2013-01-09 the FDA classified a Class II recall of Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Kehler Strabe 31 Baden-Wuerttemberg 76437 Rastatt,Germany Used to support the lower… by Maquet, citing there is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0627-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-11-02 |
| Published | 2013-01-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Maquet |
| Distribution | AR, GA, SC, TN, TX |
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 by medically trained staff within the OR environment.
Reason
There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
Identifiers
| code_info | Class I exempt Device Listing Number A922956 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0627-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.