# FDA recall Z-3025-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2020-06-22.

## 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 for recall

Sporadic problems with the current software may result in scanning workflow interruptions and unexpected user notifications causing delay in diagnosis or patient rescan

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-3025-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-22
- **Report date:** 2020-10-07
- **Termination date:** 2021-03-09

- **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-3025-2020

## Citation

> AI Analytics. FDA recall Z-3025-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-3025-2020. Source: US FDA. Licensed CC0.

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