Equate 681131228350Recalls & reported problems
Wal-Mart Stores, Inc. · Flexible Fabric Bandages, Antibacterial, all one size, 3/4 IN x 3 IN (19 mm x 76 mm) · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00681131228350), received between Nov 22, 2024 and Sep 30, 2026 — classified as 3 injuries.
The most frequently reported specific device problem is “Use of Device Problem” (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. 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 Problem2
- Use of Device Problem2
Patient problems
- Skin Inflammation/ Irritation3
- Abrasion1
- Rash1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem
On the initial report received on (b)(6) 2026, the consumer stated that she experienced a skin reaction to the bandage, including a reddish ring around the bandage. She also reported that she had already notified her physician.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 50950921 ↗InjuryJun 5, 2025Use of Device Problem; Use of Device Problem
ACCORDING TO THE INITIAL REPORT RECEIVED BY ASO ON APRIL 23, 2025, THE CONSUMER STATED THAT THE PRODUCT CAUSED HER TO EXPERIENCE A BURN OR RASH. ON THE COMPLETED CONSUMER INFORMATION REPORT (CIR) RECEIVED ON MAY 14, 2025, THE CONSUMER STATED THAT THE PRODUCT CAUSED HER TO DEVELOP A RAISED RASH, ITCH, AND SCARRING AFTER USING THE BANDAGE. CONSUMER VISITED THE RN ON (B)(6) 2025. THE RN RECOMMENDED NEOSPORIN. THE BANDAGES WERE USED TO COVER A MOSQUITO BITE. PER CIR THE ISSUE WAS WITH THE PAD AREA.
Patient problems: Rash; Skin Inflammation/ Irritation
MAUDE report 22153217 ↗InjuryNov 22, 2024Use of Device Problem; Adverse Event Without Identified Device or Use Problem; Use of Device Problem; Adverse Event Without Identified Device or Use Problem
ON THE INITIAL REPORT RECEIVED BY ASO ON 10/28/2024, THE CONSUMER STATED THAT HE HAD A BAD REACTION, HIS SKIN CAME OFF, AND HE WENT TO THE DOCTOR.
Patient problems: Abrasion; Skin Inflammation/ Irritation
MAUDE report 20762071 ↗
Other Tape And Bandage, Adhesive devices
- IV3000-1-HAND 10X12CM-CARTON OF 50 66024008Smith & Nephew Medical Limited · Tape And Bandage, Adhesive62 reports
- CURAD NON25600QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall2 reports
- 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.