Maquet Yuno Extension Table Device Maquet GmbH & Co — Class II medical device recall Z-0627-2013
Terminated recall by Maquet Inc., reported 2013-01-09, distributed in AR, GA, SC, TN, TX. There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
| Recall number | Z-0627-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Inc., Wayne, NJ, United States |
| Recall initiated | 2012-11-02 |
| Classified | 2013-01-03 |
| Reported by FDA | 2013-01-09 |
| Terminated | 2013-08-21 |
| Distributed | AR, GA, SC, TN, TX |
| Countries outside the US | AE, AU, BR, CA, CH, CN, DE, ES, FR, GB, IT, JP, RS, SE, TH, TR, ZA |
| Quantity | 63 devices |
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 for recall
There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0627-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.