# FDA recall Z-1940-2018

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2018-04-20.

## Product

SOMATOM Go.Up, Material Number 11061628    There is a potential for a software issue that may cause the need for necessary patient rescans.

## Reason for recall

There is a potential for a software issue that may cause the need for necessary patient rescans.

## Distribution

Worldwide Distribution: US (nationwide) including states of: AR, CA, CT, FL, GA, IL, IN, KS, KY, MO, ND, NY, OH, OK, SD, TN, TX, and VA; and countries of: Algeria, Australia, Austria, Bangladesh, Bolivia, Bosnia Herzog., Brazil, Cambodia, Chile, China, Columbia, Costa Rica, Germany, Greece, India, Indonesia, Italy, Japan, Kenya, Kuwait, Lithuania, Mauritius, Morocco, Nepal, Pakistan, Paraguay, Philippines, Poland, Portugal, Republic Korea, Romania, Senegal, Singapore, Slovakia, South Africa, Spain, Switzerland, Thailand, Turkey, Ukraine, and United Kingdom.

## Key facts

- **Recall number:** Z-1940-2018
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-04-20
- **Report date:** 2018-06-06
- **Termination date:** 2019-05-23

- **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-1940-2018

## Citation

> AI Analytics. FDA recall Z-1940-2018. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/Z-1940-2018. Source: US FDA. Licensed CC0.

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