Reliance Vision Single Chamber (REF FH05063)Recalls & reported problems
Corporation Steris Canada · The Reliance Vision Single-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), theater shoes and other similar and related items 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 00724995192679), received between Jul 5, 2024 and Jul 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT AN EMPLOYEE NOTICED THAT A RACK TO THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR WAS NOT MOVING FORWARD ON THE CONVEYOR, AND THEY ATTEMPTED TO MANUALLY MOVE THE RACK. THE RACK MOVED FORWARD AS THE EMPLOYEE WAS PULLING ON IT AND THEN CONTACTED THE EMPLOYEE ON THE HEAD. THE USER FACILITY DID NOT DISCLOSE THE DETAILS OF THE INJURY OR IF ANY MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Insufficient Information
MAUDE report 19679748 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.