Walgreens 400577Recalls & reported problems
Walgreen CO. · Assorted, Blister Cushions, 0.67 IN x 1.89 IN (17 mm x 48 mm); 0.63 IN x 2.36 IN (16 mm x 60 mm); 1.65 IN x 2.67 IN (42 mm x 68 mm) · Class 1
- 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 00311917195667), received between Feb 24, 2026 and Feb 24, 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
- Abrasion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2026Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE INITIAL REPORT RECEIVED ON JANUARY 13, 2026, THE CONSUMER STATED THAT THE PRODUCT CAUSED INJURED ON HER TOE AFTER RUNNING A MARATHON. IN THE COMPLETED CUSTOMER INFORMATION REQUEST (CIR) FORM SUBMITTED ON (B)(6) 2026, THE CONSUMER REPORTED THAT SHE WRAPPED THE PRODUCT AROUND HER RIGHT FOOT, AS SHE ALWAYS DOES, AND RAN A MARATHON. SHE EXPERIENCED STINGING PAIN DURING THE RUN; UPON FINISHING AND REMOVING HER SHOES, SHE NOTICED THAT HER FOOT WAS BLEEDING. THE CONSUMER WENT TO THE MEDIC TENT, AND WAS INFORMED THAT THE PLASTER HAD RIPPED OFF HER SKIN DURING THE RUN, CAUSING A DEEP ABRASION. THE CONSUMER CONFIRMED THAT THE SYMPTOMS CORRECTED AFTER SHE STOPPED USING THE PRODUCT. THE AREA HAS BEEN TREATED, AND THE WOUND IS HEALING.
Patient problems: Abrasion
MAUDE report 24427740 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.