Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table… — Class II medical device recall Z-2108-2012
Terminated recall by Maquet Medical Systems, Usa, reported 2012-08-08, distributed nationwide. As a result of a small number of customer complaints, MAQUET conducted an investigation and identified a poten
| Recall number | Z-2108-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Medical Systems, Usa, Wayne, NJ, United States |
| Recall initiated | 2012-04-13 |
| Classified | 2012-07-30 |
| Reported by FDA | 2012-08-08 |
| Terminated | 2013-09-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BR, CA, CH, CN, DE, DK, ES, FR, HK, IE, IL, IN, IT, JP, KR, NL, PL, RU, SA, SE, SG, TH |
| Model numbers | 1180.16F2, 1180.16F3, 1180.16F5, T285.7000 |
Product
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 the surgical phase. The table top is radiotranslucent and enables intraoperative use of X-ray equipment.
Reason for recall
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.
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-2108-2012. 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.