3M™ Tegaderm™ 1629Recalls & reported problems
3m Company · 3M™ Tegaderm™ Transparent Film Dressing Frame Style 1629 · 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 04001895928741), received between May 24, 2019 and May 24, 2019 — 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
- Itching Sensation1
- Peeling1
- Rash1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 24, 2019Patient Device Interaction Problem; Patient Device Interaction Problem
A CONSUMER REPORTED A PHYSICIAN APPLIED A 1629 TEGADERM¿ TRANSPARENT FILM DRESSING DURING HIS FOLLOW-UP APPOINTMENT. THE DRESSING WAS REPORTEDLY APPLIED TO HIS BACK, OVER HIS SPINAL STIMULATOR IMPLANT INCISION. THE CONSUMER REPORTED HE EXPERIENCED ITCHING AND A RASH 1.5 DAYS FOLLOWING THE DRESSING APPLICATION. HIS WIFE REPORTEDLY REMOVED THE DRESSING AND SKIN REMOVAL OCCURRED IN SOME AREAS NEAR THE LOWER PORTION OF WHERE THE DRESSING HAD BEEN APPLIED. THE CONSUMER WAS SEEN BY HIS PHYSICIAN AND WAS TREATED WITH AN RX FOR METHYLPREDNISOLONE (4MG) (ORAL DOSE PACK). THE CONSUMER WAS ALSO INSTRUCTED TO USE AN OTC OINTMENT DESCRIBED AS A THICK PASTE. THE CONSUMER REPORTED THE OPEN AREAS WERE HEALING, BUT STILL TENDER.
Patient problems: Itching Sensation; Peeling; Rash
MAUDE report 8641151 ↗
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- DUODERM 187662Convatec, Purchasing Department · Dressing, Wound, Occlusive43 reports
- ALLEVYN LIFE L 15.4X15.4 CTN10 66801069Smith & Nephew Medical Limited · Dressing, Wound, Occlusive28 reports
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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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