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Steri-Drape™ 2045Recalls & reported problems

3m Company · 2045 S-DRAPE 2 SURGICAL 10/BX · Class 2

All models of Steri-Drape (11)

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 30707387018628), received between Mar 16, 2018 and Mar 16, 2018 — 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

  • Skin Tears1

Recent adverse event reports

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

  • InjuryMar 16, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A HOSPITAL EMPLOYEE REPORTED A PATIENT EXPERIENCED A SKIN INJURY WHEN A 2045 3M¿ STERI-DRAPE¿ 2 INCISE DRAPE WAS REMOVED FOLLOWING A LAPAROTOMY PROCEDURE.

    Patient problems: Skin Tears

    MAUDE report 7346369 ↗

Other Drape, surgical, exempt devices

All Drape, surgical, exempt devices →

Sources and updates

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