CVS Health 893118Recalls & reported problems
Woonsocket Prescription Center, Incorporated · Hydrocolloid Gel Adhesive Pads, all one size, 3.07 IN x 2.32 IN (78 mm x 59 mm) · Class 1
All models of CVS Health (16)
Data updated Oct 18, 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 00050428251966), received between May 29, 2025 and May 29, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Rash1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE INITIAL REPORT DATED ON (B)(6) 2025, THE CONSUMER STATED THAT THE PRODUCT CAUSED HER BURNS. SHE HAD TO TAKE PREDNISONE, AND HER WOUND WAS STILL HEALING, AND SHE HAD A DISCOLORATION ON HER LEG. ON THE COMPLETED CIR RECEIVED VIA EMAIL FROM THE CONSUMER ON MAY 2, 2025, THE CONSUMER STATES THAT THE ENTIRE AREA OF THE BANDAGE WOUND HAS BLISTERS AND A RAISED SKIN RASH. THE CONSUMER VISITED THE DOCTOR AND WAS PRESCRIBED PREDNISONE 10MG TABLETS, HYDROXYZINE HCI 25MG, AND BETAMETHASONE VALERATE 0.1% TOPICAL CREAM.
Patient problems: Rash
MAUDE report 22105935 ↗
Other Dressing, Wound, Occlusive devices
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- DUODERM 187955Convatec, Purchasing Department · Dressing, Wound, Occlusive1 recall2,348 reports
- DUODERM 187660Convatec, Purchasing Department · Dressing, Wound, Occlusive207 reports
- DUODERM 187961Convatec, Purchasing Department · Dressing, Wound, Occlusive153 reports
- SAM Chest Seal CS203-ENSAM Medical Products · Dressing, Wound, Occlusive1 recall0 reports
- FORWARD Gunshot Wound Kit ATF-GSWIntegrated Medcraft LLC · Dressing, Wound, Occlusive1 recall0 reports
- DUODERM 187662Convatec, Purchasing Department · Dressing, Wound, Occlusive43 reports
- ALLEVYN LIFE L 15.4X15.4 CTN10 66801069Smith & Nephew Medical Limited · Dressing, Wound, Occlusive28 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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