TopCare health 036800403093Recalls & reported problems
Topco Associates, LLC · Sterile Antibacterial Extra Large Sheer Bandages, all one size, 2 IN x 4 IN · Class 1
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 00036800403093), received between Sep 20, 2015 and Sep 20, 2015 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Itching Sensation1
- Swelling1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 20, 2015Insufficient Device Problem Information
I HAD SCRAPED THE BACK OF MY FOOT AND SO I PUT A TOPCARE BRAND SHEER BANDAGE ON IT. I LEFT THE BANDAGE ON FOR 2 OR 3 DAYS BEFORE I REMOVED IT. AFTER I REMOVED THE BANDAGE. I NOTICE THAT THERE WERE RED ITCHY BUMPS AROUND THE AREA WHERE THE BANDAGE HAD BEEN. THOSE BUMPS WERE NOT THERE BEFORE I PUT THE BANDAGE ON AND ARE STILL THERE 3 DAYS AFTER I TOOK THE BANDAGE OFF.
Patient problems: Itching Sensation; Swelling
MAUDE report 5104686 ↗
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- IV3000-1-HAND 6X7CM-CARTON OF 100 66024007Smith & Nephew Medical Limited · Tape And Bandage, Adhesive52 reports
- 3M™ 1500U3m Company · Tape and bandage, adhesive1 recall1 report
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
- CURAD NON256133QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall0 reports
- CURAD NON25660QSMedline Industries, 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 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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