Equate 681131349826Recalls & reported problems
Wal-Mart Stores, Inc. · Watershield Plus Antibacterial Adhesive Bandages, assorted sizes,3/4 IN x 1-1/2 IN (19 mm x 38 mm), 3/4 IN x 2 IN (19 mm x 50 mm), 1 IN x 2-1/2 IN ( 25 mm x 63 mm) · Class 1
Data updated Oct 13, 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 00681131349826), received between Mar 5, 2026 and Mar 5, 2026 — 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
- Blister1
- 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.
InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE INITIAL REPORT RECEIVED BY THE FDA ON JANUARY 12, 2026, A CONSUMER FILED A VOLUNTARY MDR (REPORT #MW5180820). THE CONSUMER STATED THAT SHE USED THE PRODUCT TO COVER A SPOT ON HER SON'S FACE TO PREVENT INFECTION. THE FOLLOWING DAY, THE DAYCARE SENT A PHOTOGRAPH SHOWING THAT THE SKIN WHERE THE BANDAGE HAD BEEN APPLIED WAS "BUBBLED UP." THE CONSUMER STATED THAT THE BANDAGE CAUSED A CHEMICAL BURN. ON THE COMPLETED CONSUMER INFORMATION REQUEST FORM (CIR) RECEIVED ON FEBRUARY 06, 2026, THE CONSUMER STATES THAT HER SON HAD A BLEMISH ON FACE AND SHE USED THE BANDAGE TO COVER IT. A DAY LATER, HIS FACE WAS BUBBLED/BLISTERED. THE PATIENT WAS EVALUATED BY A PEDIATRICIAN, WHO PRESCRIBED AN ANTIBIOTIC AND A STEROID OINTMENT. THE CONSUMER SPECIFIED THE REACTION OCCURRED IN THE AREA OF THE ADHESIVE TAPE. WHILE THE CONSUMER CONFIRMED THAT SYMPTOMS IMPROVED AFTER DISCONTINUING PRODUCT USE, SHE NOTED THAT THE AREA IS NOT YET FULLY HEALED.
Patient problems: Blister; Skin Inflammation/ Irritation
MAUDE report 24519925 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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