PolyMemRecalls & reported problems
Ferris Mfg. Corp. · 4" x 4" PolyMem Non-Adhesive Pad Dressing · Class 1
Data updated Oct 16, 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 10735471050441), received between Aug 28, 2025 and Aug 28, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- Skin Tears1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
IT WAS REPORTED POLYMEM ADHERED TO THE PATIENT'S WOUND AND WAS UNABLE TO BE REMOVED WITH SALINE, THUS REQUIRING MANUAL DÉBRIDEMENT WITH A DERMAL CURETTE. THE HEALTHCARE PROFESSIONAL OBSERVED HEALTHY EPITHELIAL TISSUE AFTER DRESSING REMOVAL.
Patient problems: Skin Tears
MAUDE report 22917291 ↗
Other Bandage, Liquid devices
- 3M™ Cavilon™ 50503m Company · Bandage, liquid4 reports
- 3M™ Cavilon™ 33453m Company · Bandage, liquid3 reports
- MEDLINE INDUSTRIES, INC. MSC093001Medline Industries, Inc. · Bandage, liquid2 reports
- 3M™ Cavilon™ 33443m Company · Bandage, liquid2 reports
- 3M™ Cavilon™ 33423m Company · Bandage, liquid1 report
- 3M™ Cavilon™ 5051G3m Company · Bandage, liquid1 report
- 3M™ Cavilon™ 3343K3m Company · Bandage, liquid1 report
- Curity 6114Cardinal Health, Inc. · Bandage, liquid1 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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page