Magnus Hybrid OR Table Column — Class II medical device recall Z-2097-2015
Terminated recall by Maquet Cardiovascular Us Sales, Llc, reported 2015-07-29, distributed nationwide. There is a potential issue that could result to collision between the C-arm of the angiography system and the
| Recall number | Z-2097-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular Us Sales, Llc, Wayne, NJ, United States |
| Recall initiated | 2015-06-10 |
| Classified | 2015-07-17 |
| Reported by FDA | 2015-07-29 |
| Terminated | 2016-04-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, BR, CH, CL, CN, DE, ES, FR, GB, HK, IE, IL, IN, IT, JP, KW, MX, NL, NO, RU, SE, TR, TW, ZA |
| Quantity | 12 units |
Product
Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego Angiography System. Maquet GmbH & Co.
Reason for recall
There is a potential issue that could result to collision between the C-arm of the angiography system and the MAGNUS OR table system. After switching on the angiography-system, in rare cases, MAGNUS column provides wrong position data for the longitudinal movement leading to a collision.
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-2097-2015. 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.