Tegaderm™ 1660Recalls & reported problems
3m Company · 3M™ Tegaderm™ CHG Dressing 25/Carton 4 Cartons/Case 1660 · Class U
All models of Tegaderm (4)
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 30707387583911), received between Jan 17, 2019 and Jan 17, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Improper or Incorrect Procedure or Method1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 17, 2019Improper or Incorrect Procedure or Method; Adverse Event Without Identified Device or Use Problem; Improper or Incorrect Procedure or Method; Adverse Event Without Identified Device or Use Problem
A HOSPITAL REPORTED FOUR PEDIATRIC PATIENTS EXPERIENCED DISLODGEMENT OF THEIR NEWLY INSERTED TUNNELED CENTRAL CATHETERS. 1660 3M¿ TEGADERM¿ CHG CHLORHEXIDINE GLUCONATE I.V. SECUREMENT DRESSINGS WERE REPORTEDLY APPLIED TO THE CATHETER SITES. THE TUNNELED CENTRAL CATHETER CUFFS WERE NOTED TO BE EXPOSED WHEN THE DRESSINGS WERE REMOVED. NO INDIVIDUAL PATIENT INFORMATION WAS AVAILABLE. AT LEAST TWO OF THE PATIENTS REQUIRED REINSERTION OF THEIR TUNNELED CENTRAL CATHETERS.
Patient problems: No Code Available
MAUDE report 8256951 ↗
Other Dressing, wound, drug devices
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- MediHoney® 31805Acell, Inc. · Dressing, wound, drug2 recalls1 death5 reports
- MediHoney® 31535Acell, Inc. · Dressing, wound, drug2 recalls0 reports
- AQUACEL AG FOAM 420681Convatec, Purchasing Department · Dressing, Wound, Drug99 reports
- SteriCare Solutions 6240Nurse Assist, Inc. · Dressing, Wound, Drug1 recall14 reports
- Medline DYND500MLSMedline Industries, Inc. · Dressing, wound, drug1 recall5 reports
- MEDLINE MNK0005Medline Industries, Inc. · Dressing, wound, drug1 recall5 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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