Skip to content

Spirit® Hydrocolloid Adhesive Sheath 37101Recalls & reported problems

C. R. Bard, Inc. · Spirit® Hydrocolloid Adhesive Sheath · Class 1

All models of Spirit Hydrocolloid Adhesive Sheath (28)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00801741071126), received between Dec 5, 2017 and Dec 5, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Difficult to Remove1

Patient problems

  • Pain1

Recent adverse event reports

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

  • MalfunctionDec 5, 2017Difficult to Remove

    IT WAS REPORTED THAT THE ADHESIVE OF THE CATHETER WAS TOO STRONG. THE PATIENT EXPERIENCED PAIN WHILE REMOVING THE CATHETER.

    Patient problems: Pain

    MAUDE report 7082450 ↗

Other DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE devices

All DEVICE, INCONTINENCE, UROSHEATH TYPE, NON-STERILE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page