Kendall 6640Recalls & reported problems
Cardinal Health, Inc. · Transparent Film Dressing,Moisture Vapor Permeable · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 40884521007544), received between Oct 12, 2017 and Oct 12, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Sticking” (1 report).
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
Device problems
- Sticking1
Patient problems
- Skin Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 12, 2017Sticking; Sticking
THE CUSTOMER REPORTED WHEN THE DRESSING WAS REMOVED, SKIN WAS COMING OFF AS WELL. THE PATIENT WAS NOT HARMED AND NO MEDICAL INTERVENTION OR TREATMENT WAS REQUIRED.
Patient problems: Skin Irritation
MAUDE report 6945658 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.