Data Foundry

Medical device recalls 2023

Reliance Vision Multi-Chamber Washer/Disinfector — Class II medical device recall Z-1595-2023

Ongoing recall by Steris Corporation, reported 2023-05-24, distributed nationwide. In the remote occurrence in which the electrical contactor component present in the drying chambers of the Rel

Recall numberZ-1595-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSteris Corporation, Mentor, OH, United States
Recall initiated2023-04-10
Classified2023-05-17
Reported by FDA2023-05-24
DistributedNationwide (US)
Countries outside the USAU, BH, BR, CA, CH, CN, ES, GB, HK, KR, LT, NZ, QA, SA, TW, ZA
Quantity322 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00724995193164, 00980000006458, 00980000006502
Serial numbers21361632135, 3600416016, 3600622024, 3600714004, 3600908001, 3600908011, 3601011012, 3601014015, 3601017002, 3601210008, 3601215025, 3601414005, 3601822001, 3602108001, 3602108005, 3602110011, 3602114001, 3602213002, 3602323012, 3602411012, 3602511011, 3602512001, 3602517002, 3602609007, 3602714001 and 297 more

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1595-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.