Multi Display Manager in the Artis Systems — Class II medical device recall Z-2302-2020
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2020-06-17, distributed nationwide. Artis systems containing a Multi Display Manager of a specific lot, the power distributor may lead to an incre
| Recall number | Z-2302-2020 |
|---|---|
| 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 | 2020-04-30 |
| Classified | 2020-06-09 |
| Reported by FDA | 2020-06-17 |
| Terminated | 2020-09-11 |
| Distributed | Nationwide (US) |
| Quantity | 15 us |
| Serial numbers | 103335, 103340, 109620, 109621, 121518, 121520, 121521, 121525, 121526, 125253, 125254, 136555, 138311, 147237, 148418 |
| Model numbers | 10094135, 10094137, 10848280, 10848281, 10848282 |
Product
Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic X-Ray System) as follows: Artis Q floor Model: 10848280; Artis Q ceiling Model: 10848281; Artis Q biplane Model:10848282; Artis zee ceiling Model: 10094137; Artis zee floor Model: 10094135 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Reason for recall
Artis systems containing a Multi Display Manager of a specific lot, the power distributor may lead to an increased electrical contact resistance or the interruption of electrical contact, and result in planned procedures to be terminated and performed on an alternative x-ray system
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-2302-2020. 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.