VERIFY PCC071Recalls & reported problems
Steris Corporation · The VERIFY VH202 Indicator Tape is intended to secure items wrapped in synthetic wrap materials until used and to distinguish between processed and unprocessed units through a color change. It can be changed in all V-PRO Low Temperature Sterilization Systems and Sterrad 100S, NX and 100NX Sterilizers. · 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 10724995172593), received between Dec 12, 2024 and Dec 12, 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
- 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.
MalfunctionDec 12, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED VIA A VIGILANCE REPORT TO THE ITALIAN MINISTRY OF HEALTH THAT THEIR INDICATOR TAPE WAS DETACHING FROM THE STERILE BARRIER SYSTEM DURING THE STERILIZATION PHASE AND THE TAPE DID NOT CHANGE COMPLETELY. THE USER FACILITY REPORTED THAT THE DEVICES WERE REPROCESSED PRIOR TO USE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20919922 ↗
Other Indicator, physical/chemical sterilization process devices
- Integron® IT26-CTerragene S.A. · Indicator, Physical/Chemical Sterilization Process1 recall5 reports
- BENCO 5726-583Benco Dental Supply CO. · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
- 3M™ Attest™ 1243A3m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- 3M™ Attest™ 1243B3m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- DH Nyclave Indicator Labels 116312Young Dental Manufacturing I, LLC · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
- Comply™ 12483m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- Comply™ 12483m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- Integron® IT26-CTerragene S.A. · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.