Medline MSC1500Recalls & reported problems
Medline Industries, Inc. · WIPE,PROTECTANT,SKIN,SUREPREP · 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 10080196669035), received between Jan 5, 2023 and Jan 5, 2023 — 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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
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.
InjuryJan 5, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER ON (B)(6) 2022 THEY WERE USING THE SUREPREP WIPE ON THEIR MID-ABDOMEN WHEN THEY EXPERIENCED A RASH.
Patient problems: Rash
MAUDE report 16110299 ↗
Other Bandage, liquid, skin protectant devices
- APLICARE APLS1106Medline Industries, Inc. · Bandage, liquid, skin protectant4 reports
- No Sting Skin-Prep Prot. Spray 28ml US 66800709Smith & Nephew Medical Limited · Bandage, Liquid, Skin Protectant2 reports
- Protective Barrier Film 740013C. R. Bard, Inc. · Bandage, liquid, skin protectant2 reports
- SKIN-PREP Wipes 420400, 420471Smith & Nephew Medical Limited · Bandage, Liquid, Skin Protectant1 report
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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