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REMOVE Adhesive Remover 8oz US 403300Recalls & reported problems

Smith & Nephew Medical Limited · Universal adhesive remover spray · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00040565112435), received between Dec 9, 2021 and Dec 9, 2021 — classified as 1 injury.

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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Burn(s)1

Recent adverse event reports

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

  • InjuryDec 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT, DURING WOUND TREATMENT, ONE PATIENT EXPERIENCED BURNS WHEN USING REMOVE. IT IS USED THE ADHESIVE REMOVER, CHLORHEXIDINE, THEN CHLORAPREP, AND THE BURN IS ON THE SIDE OF THE PATIENT WHERE THIS MIGHT HAVE POOLED. A PAD THAT CIRCULATES HEATED WATER TO HELP WITH BODY TEMPERATURE DURING THE HEART SURGERY IS ALSO LAID. IT IS UNKNOWN HOW THIS EVENT HAS BEEN ADDRESSED. PATIENT OUTCOME IS ALSO UNKNOWN.

    Patient problems: Burn(s)

    MAUDE report 12972106 ↗

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Sources and updates

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