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3M™ Nexcare™ 771-1PKRecalls & reported problems

3m Company · Nexcare™ Flexible Clear Tape 771-1PK, 1 in x 10 yds. · Class 1

All models of 3M Nexcare (10)

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 00051131204454), received between Feb 10, 2020 and Feb 10, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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

  • Patient Device Interaction Problem1

Patient problems

  • Itching Sensation1
  • Skin Irritation1

Recent adverse event reports

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

  • InjuryFeb 10, 2020Patient Device Interaction Problem; Patient Device Interaction Problem

    A CONSUMER REPORTED VIA AN ONLINE REVIEW THAT THEY APPLIED THE REFERENCED TAPE. DATE, DURATION AND LOCATION OF WEAR WERE NOT SPECIFIED. THE TAPE WAS REPORTEDLY USED TO SECURE GAUZE. THE CONSUMER ALLEGED THEY DEVELOPED CONTACT DERMATITIS DUE TO TAPE USE. NO KNOWN ALLERGIES/SKIN SENSITIVITIES WERE SPECIFIED. THE CONSUMER REPORTED THEY USED PREDNISONE TO TREAT THE REACTION. NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: Itching Sensation; Skin Irritation

    MAUDE report 9686583 ↗

Other Tape and bandage, adhesive devices

All Tape and bandage, adhesive devices →

Sources and updates

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