FDA Device recall Z-3025-2020
Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM Definition As (Model #8098027…
- FDA Device
- Class II
- terminated
- Published 2020-10-07
On 2020-10-07 the FDA classified a Class II recall of Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM Definition As (Model #8098027… by Siemens Medical Solutions Usa, citing sporadic problems with the current software may result in scanning workflow interruptions and unexpected user notifications causing delay in diagnosis or patient rescan.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3025-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-22 |
| Published | 2020-10-07 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Software versions syngo.CT VB20 or VB20_SP1 in the following systems: SOMATOM Force (Model #10742326) SOMATOM Definition As (Model #8098027) SOMATOM Definition Edge (Model #10590000) SOMATOM Definition Flash (Model #10430603) SOMATOM Drive (Model #10431700) SOMATOM Confidence (Model #10590100) SOMATOM Edge Plus (Model #10267000)
Reason
Sporadic problems with the current software may result in scanning workflow interruptions and unexpected user notifications causing delay in diagnosis or patient rescan
Identifiers
| code_info | Software versions syngo CT VB20 and syngo CT VB20_SP1 Serial Numbers: 59812 59819 59820 59823 59825 59828 64036…Software versions syngo CT VB20 and syngo CT VB20_SP1 Serial Numbers: 59812 59819 59820 59823 59825 59828 64036 64051 64064 64066 64104 64132 64148 64160 64211 64218 64221 64347 64407 64427 64498 64500 64501 64516 64519 64605 64677 64707 64712 64732 64785 64869 64924 64999 65022 65157 65159 65186 65229 65235 65238 65247 65251 65297 65299 65370 65371 65382 65443 65478 65493 65501 65515 65556 65586 65607 65611 65652 65667 65728 65768 65770 65773 65777 65793 65795 65803 65804 65805 65808 65854 65909 65926 65956 66021 66032 66062 66095 66116 66126 66150 66151 66164 66183 66188 66197 66219 66223 66225 66232 66234 66237 66248 66265 66280 66290 66308 66319 66335 66396 66403 66407 66470 66490 66498 66502 66503 66579 66612 66635 66649 66664 66677 66688 66844 66850 66859 66882 66925 66933 66969 66999 67048 67122 67133 67192 67218 67229 67232 67236 67297 67326 6736 |
|---|
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-3025-2020%22
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