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Walgreens 940856Recalls & reported problems

Walgreen CO. · Antibacterial Flexible Fabric Medium Bandages. Benzalkonium Chloride 0.8%/Antiseptic. 2 IN X 4 IN. · Class U

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00311917185002), received between Oct 15, 2019 and Sep 13, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Loss of or Failure to Bond1

Patient problems

  • Local Reaction1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 13, 2026Loss of or Failure to Bond

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50747891 ↗
  • InjuryOct 15, 2019Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE END-USER EXPERIENCED A SKIN REACTION DURING USE OF THE BANDAGE AND ANTIBIOTIC TREATMENT WAS REQUIRED.

    Patient problems: Local Reaction

    MAUDE report 9192001 ↗

Other Dressing, Wound, Drug devices

All Dressing, Wound, Drug devices →

Sources and updates

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