Kroger 041260384073Recalls & reported problems
Kroger CO., The · Antibacterial Strong Strip Bandages, all one size, 1 3/4 IN x 4 IN · Class 1
Data updated Oct 16, 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 00041260384073), received between Sep 18, 2025 and Sep 18, 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Blister1
- Burning Sensation1
- 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.
InjurySep 18, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE INITIAL REPORT RECEIVED BY ASO ON (B)(6) 2025, THE CONSUMER STATES THAT AFTER USING THE BANDAGES, HER DAUGHTER DEVELOPED A SEVERE INFECTION, WHICH HAS CAUSED HER SIGNIFICANT DISTRESS. ON THE COMPLETED CONSUMER INFORMATION REPORT (CIR) RECEIVED ON (B)(6) 2025, THE CONSUMER STATES THAT THE PRODUCT CAUSED HER DAUGHTER TO DEVELOP SKIN ERYTHEMA STREAKING UP THE ARM. CAUSED A BURN, BLISTERING AROUND THE EDGE OF WHERE THE BANDAGE WAS. PER CIR THE CONSUMER WENT TO ST. ALPHONSUS URGENT CARE, WHERE SHE WAS PRESCRIBED AMOXICILLIN-CLAVULANATE 875-125 MG PER TABLET AND TRIAMCINOLONE 0.1 % OINTMENT. THE CONSUMER STATES THAT THE ISSUE WAS WITH THE TAPE AREA AND THAT THE SYMPTOMS DID NOT CORRECT AFTER SHE STOPPED USING THE PRODUCT. SHE WAS LEFT WITH A PERMANENT SCAR.
Patient problems: Blister; Burning Sensation; Skin Inflammation/ Irritation
MAUDE report 23082695 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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