# FDA recall Z-2405-2019

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-07-31.

## Product

SOMATOM go.Top;   Models #11061648    Product Usage:  This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data

## Reason for recall

The injector holder could potentially fall off together with the injector and the storage box.

## Distribution

US Nationwide Distribution in the states  FL  KS  WI  NE  MS  OH  TX  NY  LA  IN  IL  OK  MI  GA  NJ  AK  CT  AL  MD

## Key facts

- **Recall number:** Z-2405-2019
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-31
- **Report date:** 2019-09-04
- **Termination date:** 2020-12-02

- **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-2405-2019

## Citation

> AI Analytics. FDA recall Z-2405-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2405-2019. Source: US FDA. Licensed CC0.

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