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3M™ Steri-Strip™ B1557Recalls & reported problems

3m Company · 3M™ Steri-Strip™ Blend Tone Skin Closures (non-reinforced)50 Bags/Carton 4 Cartons/Case B1557 · Class 1

Data updated Oct 18, 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 30707387416837), received between Mar 18, 2019 and Mar 18, 2019 — 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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Rash1

Recent adverse event reports

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

  • InjuryMar 18, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A CUSTOMER ALLEGED B1557 3M¿ STERI-STRIP¿ BLEND TONE SKIN CLOSURES WERE APPLIED TO PLASTIC SURGERY PATIENTS IN THE OPERATING ROOM. THE CUSTOMER ALLEGED THREE TO FOUR PATIENTS EXPERIENCED A RASH WITH USE OF THE STERI-STRIP CLOSURES. THE CUSTOMER ESTIMATED THREE OF THE FOUR PATIENTS EXPERIENCED A SIGNIFICANT SKIN RASH REQUIRING TREATMENT WITH A STEROID DOSE PACK. INDIVIDUAL PATIENT INFORMATION WAS NOT PROVIDED. THE CUSTOMER REPORTED ALL OF THE PATIENT RASHES WERE RESOLVED.

    Patient problems: Rash

    MAUDE report 8427833 ↗

Other Tape and bandage, adhesive devices

All Tape and bandage, adhesive devices →

Sources and updates

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