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Walgreens 940859Recalls & reported problems

Walgreen CO. · Antibacterial Adhesive Pads. Benzalkonium Chloride 0.8%/LARGE BANDAGES. 3 IN x 4 IN. · Class U

All models of Walgreens (38)

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

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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00311917185033), received between Oct 7, 2019 and May 14, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (2 reports).

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

  • Patient-Device Incompatibility2

Patient problems

  • Hypersensitivity/Allergic reaction1
  • Increased Sensitivity1
  • Local Reaction1
  • Skin Discoloration1

Recent adverse event reports

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

  • InjuryMay 14, 2021Patient-Device Incompatibility

    IT WAS REPORTED THAT THE END-USER EXPERIENCED A SKIN REACTION TO THE BANDAGE ADHESIVE DURING PRODUCT USE.

    Patient problems: Hypersensitivity/Allergic reaction; Skin Discoloration

    MAUDE report 11825616 ↗
  • InjuryOct 7, 2019Patient-Device Incompatibility

    IT WAS REPORTED THAT THE CUSTOMER APPLIED A BANDAGE TO HIS SKIN AND EXPERIENCED A REACTION UNDER THE ADHESIVE OF THE BANDAGE REQUIRING MEDICAL TREATMENT.

    Patient problems: Increased Sensitivity; Local Reaction

    MAUDE report 9162175 ↗

Other Dressing, Wound, Drug devices

All Dressing, Wound, Drug devices →

Sources and updates

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