CURAD NON25510Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00080196740041), received between Jun 30, 2026 and Sep 23, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (4 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 23, 2026Loss of or Failure to Bond

  This VMSR summary report covers malfunction events that occurred in Q2 of 2023. The report summarizes 2 malfunction events involving Adhesive Bandages (NON25510). Customer reported that "was there any problems with your product adhering? They just won't stay on". The reported devices were associated with lot numbers 210401, and 210402. Associated DI: (b)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50873636 ↗
• MalfunctionSep 14, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50765899 ↗
• MalfunctionSep 10, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50718111 ↗
• MalfunctionJun 30, 2026Loss of or Failure to Bond

  IT WAS REPORTED THAT THE BANDAGE DOES NOT STAY ON.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25666638 ↗