Siemens Artis zee Ceiling Systems — Class II medical device recall Z-1080-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-03-05, distributed nationwide. During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cabl
| Recall number | Z-1080-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2013-12-16 |
| Classified | 2014-02-24 |
| Reported by FDA | 2014-03-05 |
| Terminated | 2015-03-09 |
| Distributed | Nationwide (US) |
| Quantity | 284 |
Product
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Reason for recall
During the lifetime of Artis zee Ceiling systems, there is an increased wear due to potential sub-optimal cable guidance that can lead to cable damage.
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-1080-2014. 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.