Reliance Vision Multi-Chamber (REF FH83063)Recalls & reported problems
Corporation Steris Canada · The Reliance Vision Multi-Chamber Washer Disinfector Electric Unit is 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) and other related articles found in healthcare facilities. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00724995193188), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2026Insufficient Device Problem Information
THE USER FACILITY REPORTED VIA (B)(4), (B)(6) 2026 THAT THEIR RELIANCE VISION MULTI-CHAMBER WASHER/DISINFECTOR IS RECEIVING AN "PV CHEMICAL OUT OF RANGE" ALARM. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24470230 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.