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CARE SCIENCE 017276238624Recalls & reported problems

Aso LLC · Antibacterial, Flexible Fabric, Adhesive Pads, all one size, 3 IN x 4 IN (76 mm x 101 mm) · 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 00017276238624), received between Feb 10, 2025 and Feb 10, 2025 — 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.

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: 1 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: 0 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

Patient problems

  • Skin Inflammation/ 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, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ON THE INITIAL REPORT RECEIVED BY ASO ON 01/15/2025, THE CONSUMER STATED THAT AFTER USING THE BANDAGES, SHE NOTICED THE AREA GETTING REDDER AND REDDER. THE CONSUMER WENT TO THE EMERGENCY ROOM. THE NURSE PRACTITIONER AND THE DOCTOR TOLD HER THAT THEY DIDN'T THINK IT WAS ANY SPREADING INFECTION, BUT THEY THOUGHT SHE HAD SOME REACTION TO THE ADHESIVE.

    Patient problems: Skin Inflammation/ Irritation

    MAUDE report 21344408 ↗

Other Tape And Bandage, Adhesive devices

All Tape And Bandage, Adhesive devices →

Sources and updates

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