Kroger 041260384097Recalls & reported problems
Kroger CO., The · Antibacterial Plastic Bandages, all one size, 3/4 IN x 3 IN · 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 00041260384097), received between Aug 11, 2025 and Aug 11, 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
- Abrasion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 11, 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 JUNE 25, 2025, THE CONSUMER STATES THAT THE BANDAGES CAUSED HER TWO SORES. ON THE COMPLETED CIR RECEIVED BY ASO ON JULY 29, 2025, THE CONSUMER STATES THAT SHE USED THE BANDAGES TO COVER A SORE ON THE INSIDE OF HER RIGHT ANKLE TO PROTECT IT. AFTER ONE DAY, SHE REMOVED THE BANDAGE, AND HER SKIN CAME OFF WITH THE BANDAGE. CONSUMER STATED THAT THE ISSUE WAS WITH THE TAPE AREA AND THAT THE SYMPTOMS DID NOT CORRECT AFTER SHE STOPPED USING THE PRODUCT. CONSUMER INFORMED THAT SORE IS NOT HEALING AND SHE HAS BEEN TREATED WEEKLY BY HCA HEALTHONE WOUND CARE.
Patient problems: Abrasion
MAUDE report 22772203 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.