CURAD CUR45243RBRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00080196302935), received between Aug 4, 2026 and Sep 14, 2026 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 14, 2026Loss of or Failure to Bond

  It was reported that "THEY ARE NOT STICKY. FELL OFF AFTER A FEW HOURS OF WEARING."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50755479 ↗
• MalfunctionSep 10, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50716362 ↗
• InjuryAug 4, 2026Adhesive Too Strong

  According to the customer, a bandage was used after receiving a B12 injection in the customer's right hip. About 23 hours later, the customer felt irritation and soreness in the area under the bandage. Customer showered and removed the wet bandage, and in doing so, the skin on both adhesive areas came off with the bandage.

  Patient problems: Pain; Skin Burning Sensation; Skin Disorders; Skin Inflammation/ Irritation

  MAUDE report 50129936 ↗