Telfa 7539LFRecalls & reported problems
Cardinal Health, Inc. · Adhesive Island Dressing · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884527021925), received between Jan 17, 2024 and Jan 17, 2024 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 17, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED THAT ON JANUARY 03, 2024, A HOME PATIENT (HP) CALLED THEM TO REPORT THAT THEY HAD A SEVERE RASH FROM THE TELFA ISLAND DRESSING. THE PATIENT HAD TO TAKE ANTIBIOTICS.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 18525378 ↗
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- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
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- NG Strip™ NG-25Derma Sciences Canada Inc · Tape and bandage, adhesive1 recall0 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.