FDA Device recall Z-2402-2019
SOMATOM go.All
- FDA Device
- Class II
- terminated
- Published 2019-09-04
On 2019-09-04 the FDA classified a Class II recall of SOMATOM go.All 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-2402-2019 |
| 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.All; Models #11061630 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 117515 117476 117529 117517 117505 117495 117482 117496 117533 117535 |
|---|
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-2402-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.