inforMED
MalfunctionMLR

V-PRO

Received Jun 19, 2026 · Event occurred May 22, 2026

Report 3005899764-2026-00044 · MDR key 25564211

Device

Generic name

Sterilizer

Model number

MAX 2

Catalog number

VP50002101

Product problems

  • Insufficient Device Problem Information

Patient

NA · Unknown

  • Burn(s)

Narrative

Additional Manufacturer Narrative

INVESTIGATION OF THE EVENT IS CURRENTLY IN PROGRESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

Description of Event or Problem

THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A BURN TO THEIR HAND AFTER HANDLING AN INSTRUMENT TRAY THAT WAS PROCESSED IN THEIR V-PRO MAX 2 STERILIZER. IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.