3M™ Tegaderm™ 1839-2100Recalls & reported problems
3m Company · 3M™ PICC / CVC Securement Device + Tegaderm™ I.V. Advanced Securement Dressing 20/Carton 4 Cartons/Case 1839-2100 · Class 1
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 30707387769544), received between Apr 26, 2022 and Apr 26, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Patient Device Interaction Problem1
- Patient-Device Incompatibility1
Patient problems
- Dyspnea1
- Hypersensitivity/Allergic reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 26, 2022Patient-Device Incompatibility; Patient Device Interaction Problem; Patient-Device Incompatibility; Patient Device Interaction Problem
A PATIENT ALLEGED ANAPHYLAXIS AFTER USE OF 3M¿ TEGADERM¿ PICC/CVC SECUREMENT DEVICE + I.V. ADVANCED SECUREMENT DSG, 1839-2100. THE PATIENT REPORTED TROUBLE BREATHING REQUIRING ADMINISTRATION OF A EPIPEN®. PER PATIENT THEY DID NOT INFUSE MEDICATION THAT DAY; UNKNOWN IF MD WAS AWARE OR THE MEDICATION SPECIFICS. INDICATION WAS REPORTED FOR SELECTIVE DEFICIENCY OF IMMUNOGLOBULIN G(IGG) SUB CLASSES. PATIENT SPECIFICS AND MEDICAL HISTORY ARE NOT AVAILABLE. NO FURTHER INFORMATION.
Patient problems: Dyspnea; Hypersensitivity/Allergic reaction
MAUDE report 14210204 ↗
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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 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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