3M™ Ioban™ 6648EZRecalls & reported problems
3m Company · 3M™ Ioban™ 2 Antimicrobial Incise Drape, 6648EZ, 10 Each/Carton, 4 Cartons/Case · Class 2
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 30707387793105), received between Sep 13, 2021 and Sep 13, 2021 — 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
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.
InjurySep 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SKIN STRIPPING OF A TOP LAYER OF SKIN WAS REPORTED WHEN A 3M IOBAN 2 ANTIMICROBIAL INCISE DRAPE, CATALOG 6648EZ, WAS REMOVED AFTER A UNI KNEE PROCEDURE. SKIN PREPARATION INCLUDED CHLORHEXIDINE GLUCONATE, FOLLOWED BY ALCOHOL AND THEN CHLORAPREP®. TEGADERM WAS APPLIED AT THE TIME OF DRESSING ON THE SURGICAL INCISION.
Patient problems: Skin Tears
MAUDE report 12465351 ↗
Other Drape, surgical devices
- Medline DYNJP8002Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2410Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2414RMedline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2411Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2416Medline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP3008UGMedline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP2412TMedline Industries, Inc. · Drape, surgical2 recalls0 reports
- Medline DYNJP8412UGMedline Industries, Inc. · Drape, surgical2 recalls0 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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