Up&Up 245070727Recalls & reported problems
Target Corporation · Flexible Fabric Extra Large Bandages, 2 IN x 4 IN (5 cm x 10.1 cm) · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00017276226256), received between Aug 1, 2024 and Apr 28, 2026 — classified as 2 injuries.
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 Problem2
Patient problems
- Skin Inflammation/ Irritation2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 28, 2026Adverse Event Without Identified Device or Use Problem
ON THE INITIAL REPORT RECEIVED BY ASO ON (B)(6) 2026, THE CONSUMER STATED THAT THE PRODUCT CAUSED HER IRRITATION UNDER THE ARM AND ON THE LEFT SIDE OF THE BREAST. THE INCIDENT DID NOT RESULT IN HOSPITALIZATION, BUT THE CONSUMER SOUGHT PRIMARY CARE MEDICAL ATTENTION ON (B)(6) 2026.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 25015173 ↗InjuryAug 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON THE INITIAL REPORT RECEIVED BY ASO ON 09/09/2024, THE CONSUMER STATED THAT HE SOUGHT MEDICAL ATTENTION. HE WAS PRESCRIBED A STEROID TO SOOTHE THE SWELLING. ON THE COMPLETED CIR RECEIVED FROM THE CONSUMER ON 09/03/2024, THE CONSUMER STATES THAT THE PRODUCT CAUSED A DERMIC ALLERGIC REACTION. THE CONSUMER STATES THAT HE WORE THE BANDAGE FOR ONE DAY AND NOTICED SLIGHT IRRITATION UNDER IT. THE CONSUMER REPLACED THE TARGET BANDAGE WITH A WALMART BANDAGE AND CHANGED IT DAILY. THE WOUND HEALED AFTER A COUPLE OF DAYS OF WEARING THE WALMART BANDAGE. HE PEELED OFF THE BANDAGE ONCE THE CUT WAS FULLY HEALED AND DISCOVERED A PERFECT RECTANGLE OF THE ALLERGIC REACTION WITH RED SWELLING BUMPS. PER CIR, THE CONSUMER HAD TWO TELEHEALTH SESSIONS AND WAS PRESCRIBED TRIAMCINOLONE ACETONIDE CREAM USP 0.1%, A TOPICAL STEROID. THE STEROID SUCCESSFULLY STOPPED THE SWELLING ON HIS SKIN. THE REACTION LEFT A DARK RECTANGLE THAT PARTLY DISAPPEARED OVER THE LAST MONTH.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 19887521 ↗
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
- Lucky Super Soft Bandages in differenet sizeDelta Brands Inc. · Tape And Bandage, Adhesive1 recall0 reports
- 3M™ Durapore™ 1538-1183M Deutschland GmbH · Tape and bandage, adhesive1 recall0 reports
- CURAD NON256133QSMedline Industries, Inc. · 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 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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