# FDA recall Z-0265-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-09-24.

## Product

SOMATOM go.Top, Models 11061640 & 11061648-  a Computer tomography x-ray system

## Reason for recall

SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and  active  Guide&GO  license   No dose documentation and no Dose Alert for the special mode  i-  Sequence  during interventional procedures

## Distribution

US in the states of: GA, IN, MO, MS, NJ, OH, PA

## Key facts

- **Recall number:** Z-0265-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-09-24
- **Report date:** 2019-11-27
- **Termination date:** 2024-07-08

- **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-0265-2020

## Citation

> AI Analytics. FDA recall Z-0265-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0265-2020. Source: US FDA. Licensed CC0.

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