VERIFY RESI-TEST SLIDE-THRURecalls & reported problems
Steris Corporation · VERIFY RESI-TEST SLIDE-THRU Brush -2.6-5.0mm, 290cm length is designed to detect a broad spectrum of protein residues and is intended for use after manual or automated cleaning and prior to high level disinfection or sterilization. · 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 00724995231934), received between May 26, 2026 and May 26, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Scratched Material” (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
- Scratched Material1
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.
MalfunctionMay 26, 2026Scratched Material
THE USER FACILITY REPORTED VIA (B)(4), THAT "IT WAS DISCOVERED WHILE REPROCESSING AN ENDOSCOPE THE RESI TEST BRUSH WAS SHREDDING WHEN BEING PLACED THROUGH THE SCOPE." NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25280281 ↗
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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