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Kendall 2531CRecalls & reported problems

Cardinal Health, Inc. · Standard Porous Tape · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521138797), received between Jun 3, 2021 and Jul 28, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Separation Problem” (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

  • Adverse Event Without Identified Device or Use Problem1
  • Separation Problem1

Patient problems

  • Hypersensitivity/Allergic reaction1
  • Skin Tears1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 28, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE CUSTOMER REPORTED THAT THEY HAVE HAD A STAFF MEMBER EXPERIENCE ANAPHYLAXIS REACTION. THE CUSTOMER WANTED TO INQUIRE IF THE ITEM CONTAINED LATEX BECAUSE THE BROCHURE SHOWS IT IN FACT CONTAINS LATEX YET THE PICTURE ON THE SITE SAYS HYPOALLERGENIC.

    Patient problems: Hypersensitivity/Allergic reaction

    MAUDE report 15121245 ↗
  • MalfunctionJun 3, 2021Separation Problem; Separation Problem

    THE CUSTOMER REPORTED THAT THE TAPE IS PULLING THE SKIN OFF WHEN BEING REMOVED FROM THE ANIMAL WHEN USED IN A VETERINARY SETTING.

    Patient problems: Skin Tears

    MAUDE report 11936050 ↗

Other Tape And Bandage, Adhesive devices

All Tape And Bandage, Adhesive devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.