Ioban™ 2 6640Recalls & reported problems
3m Company · 3M™ Ioban™ 2 Antimicrobial Incise Drape 6640 · Class 2
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 30707387444380), received between Sep 23, 2022 and Sep 23, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Patient Device Interaction 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 23, 2022Patient Device Interaction Problem; Patient Device Interaction Problem
A 6-MONTH-OLD ALLEGEDLY EXPERIENCED LEFT CHEST SUPERFICIAL SKIN TEARS WITH POST OPERATIVE REMOVAL OF 3M¿ IOBAN¿ 2 ANTIMICROBIAL INCISE DRAPE, 6640. THE ALLEGED SKIN TEARS WERE DRESSED WITH DUODERM® DRESSINGS AND TREATED WITH MUPIROCIN ANTIBIOTIC TOPICAL OINTMENT WITH WOUND CARE. UPON DISCHARGE, THE SKIN TEAR AREA REPORTEDLY APPEARED PINK WITH A SCAB AND NO SIGNS OF INFECTION.
Patient problems: Skin Tears
MAUDE report 15469737 ↗
Other Drape, surgical devices
- Medline DYNJP8002Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2414RMedline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2411Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2410Medline Industries, Inc. · Drape, surgical2 recalls2 reports
- Medline DYNJP2416Medline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP3008UGMedline Industries, Inc. · Drape, surgical2 recalls1 report
- Medline DYNJP8201UGMedline Industries, Inc. · Drape, surgical2 recalls0 reports
- Medline DYNJP2412TMedline 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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page