3M™ Tegaderm™ 1683Recalls & reported problems
3M Deutschland GmbH · 3M™ Tegaderm™ I.V. Advanced Securement Dressing, 1683, 2-1/2 in x 2-3/4 in, 6.5 cm x 7 cm, 100/ct 4ct/Case · Class 1
- 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 00707387808150), received between Nov 14, 2025 and Nov 14, 2025 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT RECEIVED INTRAVENOUS FLUID THERAPY VIA AN INDWELLING INTRAVENOUS NEEDLE, SECURED WITH A 3M¿ TEGADERM¿ I.V. ADVANCED SECUREMENT DRESSING. APPROXIMATELY ONE HOUR AFTER APPLICATION, THE PATIENT DEVELOPED SKIN FLUSHING SPREADING FROM THE LEFT HAND TO THE ENTIRE LEFT UPPER LIMB, ACCOMPANIED BY SCATTERED MILLET-LIKE PAPULES AND ITCHY SKIN. THE TRANSPARENT DRESSING WAS IMMEDIATELY REPLACED WITH ADHESIVE TAPE FOR FIXATION. THE ATTENDING PHYSICIAN WAS NOTIFIED AND A 0.9% SODIUM CHLORIDE INJECTION AND 10MG DEXAMETHASONE SODIUM PHOSPHATE INJECTION WERE ADMINISTERED INTRAVENOUSLY. APPROXIMATELY 30 MINUTES AFTER MEDICATION, THE PATIENT¿S ITCHING GRADUALLY SUBSIDED, AND THE RASH RESOLVED WITHIN ABOUT 2 HOURS. NO RECURRENCE OF SYMPTOMS WAS OBSERVED AFTER THE ADHESIVE TAPE WAS USED FOR FIXATION.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 23558542 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.