FDA Device recall Z-0876-2021
Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate level disinfection of…
- FDA Device
- Class II
- terminated
- Published 2021-01-27
On 2021-01-27 the FDA classified a Class II recall of Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate level disinfection of… by Steris, citing the electrical contactor component present in the drying chamber of the Reliance Vision Single-Chamber Washer/Disinfector may malfunction, potentially leading to the heating eleme….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0876-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-12-11 |
| Published | 2021-01-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Steris |
| Distribution | US |
Product
Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments, such as forceps and clamps, theatre shoes, and other similar and related articles found in healthcare facilities.
Reason
The electrical contactor component present in the drying chamber of the Reliance Vision Single-Chamber Washer/Disinfector may malfunction, potentially leading to the heating elements in the drying chamber to overheat, eventually resulting in smoke and/or fire.
Identifiers
| code_info | Serial numbers: 361419028 3604919028 3610519017 3617619013 3625814030 3631216024 3600311010 3605009010 3610519018 3…Serial numbers: 361419028 3604919028 3610519017 3617619013 3625814030 3631216024 3600311010 3605009010 3610519018 3617619014 3625814031 3631216027 3600312001 3605010015 3610519019 3617619015 3625910009 3631216028 3600312004 3605018022 3610519020 3617619016 3625913019 3631216029 3600312017 3605018023 3610520002 3617717009 3625913020 3631309006 3600312018 3605018024 3610520003 3617717010 3625913021 3631310001 3600317007 3605018025 3610520004 3617717011 3625913022 3631311001 3600317008 3605018026 3610520005 3617717020 3625913023 3631311002 3600317015 3605018027 3610618018 3617717021 3625913024 3631315020 3600317016 3605112002 3610618019 3617718012 3625913025 3631315021 3600317017 3605112003 3610618025 3617718013 3625913026 3631315022 3600317018 3605112026 3610618026 3617718014 3625913027 3631315023 3600317019 3605112027 3610618031 3617718015 3625913028 3631315024 3600318002 3605112029 3610709001 3617718016 3625916002 3631315025 3600318004 3605112030 3610712001 3617811002 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0876-2021%22
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