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Curity 44101Recalls & reported problems

Cardinal Health, Inc. · Flexible Adhesive Bandage · 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 10884521144477), received between Jun 1, 2018 and Jun 1, 2018 — 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

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 1, 2018Sticking; Sticking

    THE CUSTOMER REPORTED THE ADHESIVE WAS STICKIER THAN NORMAL. IT WASN'T COMING OUT EASILY. WHEN THE PATIENT REMOVED IT FINALLY, IT DISCOLORED HER SKIN AND LEFT A DARK PATCH ON THE SKIN WHICH CAME IN CONTACT WITH THE ADHESIVE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7561064 ↗

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.