Reliance Vision Multi-Chamber (REF FH94062)Recalls & reported problems
Corporation Steris Canada · The Reliance Vision Multi-Chamber Washer Disinfector Sonic 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
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00724995193294), received between Aug 28, 2025 and Aug 28, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (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
- Mechanical Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 28, 2025Mechanical Problem; Mechanical Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS HANDLING A RACK TO THEIR RELIANCE VISION MULTI-CHAMBER WASHER/DISINFECTOR AND OBTAINED AN INJURY TO THEIR FINGER. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT (X-RAY).
Patient problems: Pain
MAUDE report 22912611 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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