AMSCO Drying Cabinet (REF DCR100101XL)Recalls & reported problems
Corporation Steris Canada · The AMSCO Drying Cabinet, 29-inch with Pass Through with large shelves delivers unrivaled precision with exact temperature control, timers for every shelf and HEPA filtration. · 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 00724995216290), received between Dec 22, 2025 and Dec 22, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
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.
MalfunctionDec 22, 2025Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
THE USER FACILITY REPORTED THAT WHEN AN EMPLOYEE WAS OPENING THE DOOR TO THEIR AMSCO DRYING CABINET, THE UPPER DOOR PANEL DROPPED DOWN AND CONTACTED THE EMPLOYEE'S HEAD. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT.
Patient problems: Pain
MAUDE report 23863110 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.