Walgreens 109881Recalls & reported problems
Walgreen CO. · Sheer Adhesive Pads, one size, 3 IN x 4 IN (76 mm x 101 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 00311917205458), received between Mar 10, 2025 and Mar 10, 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
- 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 10, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON THE INITIAL REPORT 09/23/2024, THE CONSUMER STATED THAT THE ADHESIVE AROUND THE PAD CAUSED IRRITATION ON THE ARM AND LEG. CONSUMER HAD A DOCTOR'S APPOINTMENT FOR ANOTHER ISSUE AND WAS TOLD TO USE AN ANTIBIOTIC OINTMENT. BEFORE THE ARM STARTED TO BREAK, THE CONSUMER USED 14 BANDAGES (2 PER DAY FOR 7 DAYS). HER ARM STARTED TO ITCH, AND SHE STARTED NOTICING LITTLE BUMPS ON HER ARM. THE CONSUMER RETURNED THE CUSTOMER INFORMATION REQUEST (CIR) ON 02/27/2025. THE CONSUMER INFORMED THAT SHE USED THE PRODUCT AFTER GREASE SPLASHED ON HER ARM AND LEG WHEN COOKING. CONSUMER STATED THAT TREATMENT WAS REQUIRED. CONSUMER WENT TO THE URGENT CARE, AND THE DOCTOR ADVISED TO GET OVER-THE-COUNTER BURN CREAM. CONSUMER STATED THAT THE ISSUE WAS WITH THE TAPE AREA. THE ADHESIVE AREA OF THE PATCH LEFT AN ALLERGIC REACTION ON HER ARM AND LEG. IN ADDITION, CONSUMER CONFIRMED THAT SYMPTOMS CORRECTED AFTER SHE STOPPED USING THE PRODUCT.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 21560949 ↗
Other Tape And Bandage, Adhesive devices
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- 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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