FDA Device recall Z-2400-2019
SOMATOM go.Up
- FDA Device
- Class II
- terminated
- Published 2019-09-04
On 2019-09-04 the FDA classified a Class II recall of SOMATOM go.Up by Siemens Medical Solutions Usa, citing the injector holder could potentially fall off together with the injector and the storage box.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2400-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-31 |
| Published | 2019-09-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
Reason
The injector holder could potentially fall off together with the injector and the storage box.
Identifiers
| code_info | Serial Number 111232 111409 111332 111370 111371 111383 111378 111352 111299 111273 111373 111289 111339 111317 111333 111297 111237 111303 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2400-2019%22
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