ABC 195515047098Recalls & reported problems
Amazon.Com Services LLC · Antibacterial Sheer Adhesive Pads, 3 in x 4 in (76 MM x 101 MM) · Class 1
- 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 00195515047098), received between Jul 9, 2025 and Jul 9, 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burning Sensation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IN THE INITIAL REPORT RECEIVED ON (B)(6) 2025, THE CONSUMER STATED THAT THE BANDAGE CAUSED A BURN ON THE LEG AND THAT MEDICAL ATTENTION WAS SOUGHT.
Patient problems: Burning Sensation
MAUDE report 22457360 ↗
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- IV3000-1-HAND 6X7CM-CARTON OF 100 66024007Smith & Nephew Medical Limited · Tape And Bandage, Adhesive52 reports
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
- 3M™ 1500U3m Company · Tape and bandage, adhesive1 recall1 report
- NG Strip™ NG-25Derma Sciences Canada Inc · Tape and bandage, adhesive1 recall0 reports
- Lucky Super Soft Bandages in differenet sizeDelta Brands Inc. · Tape And Bandage, Adhesive1 recall0 reports
- Seer Home SM-01-9005Seer Medical Holdings Limited · Tape And Bandage, Adhesive1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.