# FDA recall Z-1595-2023

> **Steris Corporation** · Class II · device recall initiated 2023-04-10.

## Product

Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062

## Reason for recall

In the remote occurrence in which the electrical contactor component present in the drying chambers of the Reliance Vision Multi-Chamber Washer/Disinfector malfunctions, the heating elements in the drying chamber could overheat, eventually resulting in smoke and/or fire.

## Distribution

Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: China, Lithuania, Saudi Arabia, Korea, Republic of, Canada, Taiwan, United Kingdom, Spain, Australia, New Zealand, Spain, Brazil, Bahrain, Switzerland, Great Britain, South Africa, Hong Kong, Qatar.

## Key facts

- **Recall number:** Z-1595-2023
- **Recalling firm:** Steris Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-10
- **Report date:** 2023-05-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1595-2023

## Citation

> AI Analytics. FDA recall Z-1595-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1595-2023. Source: US FDA. Licensed CC0.

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