CURAD NON25600QSRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20888277699400), received between May 15, 2026 and Sep 17, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Oct 27, 2025Open, Classified

   Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

   Z-0901-2026 · Root cause: Package design/selection · FDA record ↗

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 17, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50809525 ↗
• MalfunctionMay 15, 2026Loss of or Failure to Bond

  CUSTOMER STATES THIS MOST RECENT BOX OF CURAD BANDAGES I PURCHASED DOES NOT ADHERE WELL AT ALL. I'VE TRIED USING MULTIPLE BANDAGES IN HOPES THEY WOULD ADHERE TO EACH OTHER, BUT EVEN THAT IS PROVING INEFFECTIVE.

  Patient problems: Insufficient Information

  MAUDE report 25193068 ↗