FDA Device recall Z-1595-2023
Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062
- FDA Device
- Class II
- ongoing
- Published 2023-05-24
On 2023-05-24 the FDA classified a Class II recall of Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062 by Steris, citing 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 heati….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1595-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-04-10 |
| Published | 2023-05-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Steris |
| Distribution | US |
Product
Reliance Vision Multi-Chamber Washer/Disinfector, Reference Number FH83062
Reason
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.
Identifiers
| code_info | UDI-DI: 00724995193164; Serial Numbers: 3600416016 3604417032 3608519001 3616109004 3624018002 3629014002 3633013003 36…UDI-DI: 00724995193164; Serial Numbers: 3600416016 3604417032 3608519001 3616109004 3624018002 3629014002 3633013003 3600622024 3604520026 3608615002 3616111012 3624210004 3629108006 3633206001 3600714004 3604612002 3609014014 3616113019 3624521001 3629112001A 3633317002 3600908001 3604710009 3609207002 3616318001 3624616022 3629119023 3633319035 3600908011 3605009011 3609422016 3616320002 3624812020 3629217002 3633321010 3601011012 3605013002 3609512007 3616914006 3624919019 3629420002 3633511005 3601014015 3605015001 3609809008A 3616918017 3625010007 3629711013 3633514038 3601017002 3605219005 3609814014 3617007001 3625114031 3629719006 3633515002 3601210008 3605312002 3609819030 3617009001 3625213015 3629921003 3633515004 3601215025 3605317002 3610007005 3617219002 3625220019 3630214002 3633520032 3601414005 3605411007 3610108008 3617310007 3625321002A 3630218043 3633609012 3601822001 3605510007 3610113001 3617414019 3625412018 3630320001 3633613033 3602108001 3605514027 3610312006 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1595-2023%22
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