# FDA recall Z-2525-2018

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2018-05-25.

## Product

AXIOM Artis with Laird Cooling Unit for SSFD: Material # 7555118.   Artis is an angiography system developed for single and biplane diagnostic imaging and interventional procedures.

## Reason for recall

Due to a defective sealing, coolant may inflow into the electrical parts of the system cabinet, which could cause a short circuit and cause the system to shut down suddenly during an ongoing procedure

## Distribution

HI , IL, MI, NC, NY, VA, WI

## Key facts

- **Recall number:** Z-2525-2018
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-25
- **Report date:** 2018-08-01
- **Termination date:** 2019-05-16

- **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-2525-2018

## Citation

> AI Analytics. FDA recall Z-2525-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2525-2018. Source: US FDA. Licensed CC0.

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