# FDA recall Z-2848-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2020-07-14.

## Product

Cios Alpha (VA20) - Model: 10308191  Cios Alpha (VA30) - Model: 11105200  Cios Spin (VA30) -  Model: 10308194    Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications

## Reason for recall

Hardware error- Hot Plugging  feature could cause an electrical malfunction on the main control D80 (below revision 04 installed) of the generator which is part of the main unit (c-arm) and cause  permanent loss of imaging  functionality.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-2848-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-14
- **Report date:** 2020-09-02
- **Termination date:** 2021-07-23

- **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-2848-2020

## Citation

> AI Analytics. FDA recall Z-2848-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2848-2020. Source: US FDA. Licensed CC0.

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