# FDA recall Z-2240-2023

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2023-06-05.

## Product

Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive Care Station, Pediatrics, Ambulatory patient care and in Veterinary Medicine.   Material #11515088

## Reason for recall

Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of liquid following the plexiglass dropping off, at the same time the user or operator happens to touch the liquid on the cover which is connected to the internal live parts).

## Distribution

Worldwide - US Nationwide distribution in the states of FL, GA, KS, MN, NC, NY and the countries of Austria, Bangladesh, Brazil, Canada, China, Croatia, El Salvador, France,  Germany, Indonesia, Italy, Japan, Jordan, Lebanon, Luxembourg, Mauritius, Mexico,  Monaco, Peru, Philippines, Poland, Romania, Slovakia, South Africa, Spain, Switzerland,  Taiwan, Ukraine, United Kingdom.

## Key facts

- **Recall number:** Z-2240-2023
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-05
- **Report date:** 2023-08-02

- **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-2240-2023

## Citation

> AI Analytics. FDA recall Z-2240-2023. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-2240-2023. Source: US FDA. Licensed CC0.

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