MEDLINE DYN540Recalls & reported problems
Medline Industries, Inc. · HOLDER,TRACH TUBE,ADULT, TWO PIECE · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10197344103607), received between Sep 8, 2026 and Sep 15, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).
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
- Detachment of Device or Device Component2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Detachment of Device or Device Component
It was reported that the comforting piece is separating from the foam trach tie.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50766460 ↗MalfunctionSep 8, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50675662 ↗
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- Medline DYNJMBRC2Medline Industries, Inc. · DEVICE, FIXATION, TRACHEAL TUBE1 recall1 report
- Medline DYNJMBRC4BMedline Industries, Inc. · DEVICE, FIXATION, TRACHEAL TUBE1 recall0 reports
- AnchorFast 9799Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE21 reports
- HUDSON RCI IPN914324Teleflex Incorporated · DEVICE, FIXATION, TRACHEAL TUBE6 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.