# FDA recall Z-2128-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2020-04-17.

## Product

Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194

## Reason for recall

The unplugging of the main cable on the monitor trolley from the X10 connector can cause an unsafe electrical voltage (up to 67,6 V DC) at the X10 connector. This can result in an electrical shock if the user or other persons touch the contact pins of the X10 connector.

## Distribution

US Nationwide Distribution to states of:  AR, AZ, CA, FL, IL, IN, MA, MD, MI, MN, NC, NE, NH, NJ, NY, OH, OK, SC, TN, TX, UT, VA, WA, and Puerto Rico.

## Key facts

- **Recall number:** Z-2128-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-17
- **Report date:** 2020-06-03
- **Termination date:** 2020-08-25

- **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-2128-2020

## Citation

> AI Analytics. FDA recall Z-2128-2020. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/Z-2128-2020. Source: US FDA. Licensed CC0.

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