MalfunctionMLR
MAX 2
Received Nov 7, 2025 · Event occurred Oct 10, 2025
Report 3005899764-2025-00087 · MDR key 23497821
Device
Generic name
V-pro Max 2 Sterilizer,
Manufacturer
Steris Mexico, S. De R.l. De C.v.Model number
MAX 2Catalog number
VP50003201
Product problems
- Insufficient Device Problem Information
- Insufficient Device Problem Information
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
THE USER FACILITY REPORTED THAT TWO OF THEIR EMPLOYEES OBTAINED WHITE RESIDUE ON THEIR HANDS WHILE REMOVING VAPROX HC STERILANT CUPS FROM THEIR V-PRO MAX 2 STERILIZER. THE EMPLOYEES WASHED THEIR HANDS AND CONTINUED WORKING. NO REPORT OF INJURY.
Additional Manufacturer Narrative
THE VAPROX HC STERILANT CUP SUBJECT OF THE REPORTED EVENT IS BEING RETURNED FOR EVALUATION. INVESTIGATION OF THIS EVENT IS CURRENTLY IN PROCESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.