3M™ Cavilon™ 5050 (UDI 10707387810693)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10707387810693), received between Sep 19, 2025 and Sep 19, 2025 — classified as 1 injury.

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjurySep 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A CUSTOMER USED 3M¿ CAVILON¿ ADVANCED SKIN PROTECTANT WITH HER OSTOMY BAG AND EXPERIENCED ITCHY AND BRIGHT PINK SKIN. ADDITIONAL INFORMATION WAS RECEIVED FROM THE CUSTOMER ON (B)(6) 2025 INDICATING A YEAST INFECTION DEVELOPED AND TREATMENT WAS INITIATED WITH TOPICAL NYSTATIN. CHANGES WERE MADE TO THE OSTOMY WAFER APPLICATION PROCESS WITH THE HELP OF A WOUND, OSTOMY AND CONTINENCE NURSE (WOCN), AND THE SYMPTOMS IMPROVED.

  Patient problems: Fungal Infection

  MAUDE report 23095829 ↗