Siemens AXIOM Artis zee/zeego systems equipped with generator A100… — Class II medical device recall Z-1750-2013
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2013-07-24, distributed nationwide. During the course of product monitoring, Siemens became aware of a tolerance problem in the power supply of th
| Recall number | Z-1750-2013 |
|---|---|
| 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 | 2013-01-31 |
| Classified | 2013-07-17 |
| Reported by FDA | 2013-07-24 |
| Terminated | 2014-11-12 |
| Distributed | Nationwide (US) |
| Quantity | 23 |
| Reason classes | device malfunction |
| Serial numbers | 147500, 147514, 147515, 147516, 147526, 147528, 154406, 154408, 154423, 154425, 154429, 154430, 154453, 157907, 160431, 160800, 160807, 160812, 160813, 160814, 160816, 160817, 160823 |
Product
Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system
Reason for recall
During the course of product monitoring, Siemens became aware of a tolerance problem in the power supply of the generator control above a specific value, thus, the generator may fail.
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-1750-2013. 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.