AMSCO 2532 (REF FH120116)Recalls & reported problems
Corporation Steris Canada · The AMSCO 2532 Single-Chamber Washer Disinfector, Nonvented Unit with wall flange and double-doors is intended for use in the cleaning and intermediate-level disinfection of soiled reusable utensils, trays, glassware, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other similar 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 00724995192907), received between May 16, 2024 and May 16, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device 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
- Use of Device Problem1
Patient problems
- Bruise/Contusion1
- 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.
MalfunctionMay 16, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT DURING A DECONTAMINATION CYCLE FOR THEIR AMSCO 2532 SINGLE CHAMBER WASHER/DISINFECTOR, SMALL FLAMES WERE OBSERVED WITHIN THE BOTTOM OF THE CHAMBER. USER FACILITY PERSONNEL OPENED THE CHAMBER DOOR AND EXTINGUISHED THE FLAMES. NO REPORT OF INJURY.
Patient problems: Bruise/Contusion; No Clinical Signs, Symptoms or Conditions
MAUDE report 19333217 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.