FDA Device recall Z-0285-2022
SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000
- FDA Device
- Class II
- terminated
- Published 2021-12-01
On 2021-12-01 the FDA classified a Class II recall of SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 by Siemens Medical Solutions Usa, citing software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0285-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-08-30 |
| Published | 2021-12-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000
Reason
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in diagnosis, the necessity for patient rescans, and/or the need for additional contrast media may occur
Identifiers
| code_info | Serial Numbers: 155403 84012 83047 83095 83915 83801 155351 155353 83826 83754 83904 155521 83632 83743 155578 83931 83…Serial Numbers: 155403 84012 83047 83095 83915 83801 155351 155353 83826 83754 83904 155521 83632 83743 155578 83931 83979 155393 155396 155413 155489 83238 83336 83984 83401 84006 83834 83562 155341 83564 83582 155606 83596 155596 155485 155437 83934 83746 83234 83971 155573 155335 155422 83332 155459 155382 83994 83026 83330 155501 155535 83281 83767 155600 83880 83683 155360 155361 155564 83339 155580 83244 155615 83585 83899 155504 155315 83852 83226 83271 83607 84011 155405 83403 83599 155373 83937 83246 83388 83668 155343 155554 155399 83837 83591 83878 83714 155463 155447 83574 83567 83832 83886 83662 83763 83308 155312 83871 83375 83988 83227 83359 83031 155364 83520 83262 155502 84019 83903 83901 155524 84024 155513 83798 83292 83083 83096 83243 83319 83294 83544 83637 83640 83705 83707 155354 155507 83581 83717 83056 83950 155559 83382 83819 83363 83307 155388 84020 83732 83752 155581 155584 155569 155427 83961 155329 83845 83236 155318 83348 155374 155365 83846 83399 155601 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0285-2022%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.