CURAD CURCC320BCRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888277362966), received between Sep 11, 2026 and Sep 22, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (3 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2026Adhesive Too Strong

  It was reported that "I purchased this bulk pack and used a bandage which caused severe bruising to my arm after being on small cut for less than 8 hours" and "The adhesive was so strong that it created a bruise 10 times the original cut and I used a small bandage maybe 3/4\" x 3\"."

  Patient problems: Bruise/Contusion; Erythema

  MAUDE report 50852590 ↗
• MalfunctionSep 17, 2026Loss of or Failure to Bond

  It was reported that "we all have had issues with the bandages not adhering" and "I¿ve used 4 band aids and not one has adhered!" The customer further reported, "Will not adhere to skin, to prevent bleeding! Falls rig(t off !"

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50803161 ↗
• MalfunctionSep 16, 2026Adhesive Too Strong

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50790696 ↗
• MalfunctionSep 11, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50737195 ↗
• MalfunctionSep 11, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50734954 ↗