Curad CUR5115Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888277317607), received between Jan 8, 2025 and Sep 12, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 12, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50746549 ↗
• InjuryJan 8, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE CUSTOMER "I VISITED AN URGENT CARE FACILITY DUE TO SMALL (1.5 INCH ROUND) RASHES ON POSTERIOR LEFT SHIN AND LEFT SIDE HIP AREAS."

  Patient problems: Rash

  MAUDE report 21106432 ↗