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SensiClip 4403ARecalls & reported problems

Carefusion 2200, Inc · SensiClip Surgical Clipper Blade · 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 10885403473128), received between May 18, 2022 and May 18, 2022 — classified as 1 malfunction.

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

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.

  • MalfunctionMay 18, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THERE HAS BEEN AN INCREASE IN CLIPPER RAZOR BURNS. VERBATIM: INDICATES THAT THEY HAVE SEEN AN INCREASE IN CLIPPER RAZOR BURNS AND ASKED FOR A REFRESHER ON PROPER AND SAFE USE FOR THE STAFF WHO CLIPS PATIENTS PRIOR TO SURGERY.

    Patient problems: Skin Inflammation/ Irritation

    MAUDE report 14428222 ↗

Other RAZOR, SURGICAL devices

All RAZOR, SURGICAL devices →

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