Siemens Artis zee systems — Class II medical device recall Z-2340-2015
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2015-08-12, distributed nationwide. The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate t
| Recall number | Z-2340-2015 |
|---|---|
| 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 | 2015-06-29 |
| Classified | 2015-08-05 |
| Reported by FDA | 2015-08-12 |
| Terminated | 2016-12-07 |
| Distributed | Nationwide (US) |
| Serial numbers | 103001, 105007, 117001, 117006, 117009, 124002, 124006, 124007, 124015, 124034, 124039, 125000, 125002, 125003, 125004, 125005, 125006, 125008, 131000, 131005, 131006, 131011, 131013, 135000, 135102 and 475 more |
Product
Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography, general angiography, rotational angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures.
Reason for recall
The possibility exists for a large amount of liquid to seep through the top cover of the table and penetrate the components inside the table. If this occurs, table movements may no longer be possible. No injuries reported.
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-2340-2015. 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.