# FDA recall Z-0962-2022

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2022-03-07.

## Product

SIEMENS SOMATOM with software syngo CT VA30A_SP4  Models:   SOMATOM go.Now   11061610 & 11061618  SOMATOM go.Up   11061620 & 11061628  SOMATOM go.All   11061630 & 11061638  SOMATOM go.Top   11061640 & 11061648  SOMATOM go.Sim   11061660 & 11061668  SOMATOM go.Open Pro   11061670 & 11061678  SOMATOM X.cite   11330001  Intended Use: Computed tomography x-ray system

## Reason for recall

Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during interventional workflows.  Results in potential patient issues: Possible rescan ,  Unexpected X-Ray dose and additional contrast media, Delay in diagnosis, scan abort,and patient rescan

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-0962-2022
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-03-07
- **Report date:** 2022-04-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0962-2022

## Citation

> AI Analytics. FDA recall Z-0962-2022. Retrieved 2026-08-24 from https://api.ai-analytics.org/recall/Z-0962-2022. Source: US FDA. Licensed CC0.

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