MEDLINE DYN542Recalls & reported problems
Medline Industries, Inc. · HOLDER,TRACH TUBE, NEONATE, TWO PIECE · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10197344103621), received between Aug 13, 2026 and Sep 29, 2026 — classified as 3 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
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932808 ↗MalfunctionSep 22, 2026Detachment of Device or Device Component
It was reported that Trach Tie seems to be coming apart from the foam.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856162 ↗MalfunctionAug 13, 2026Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50240594 ↗
Other DEVICE, FIXATION, TRACHEAL TUBE devices
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- AnchorFast SlimFit 9787Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall4 reports
- AnchorFast Guard 9800Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall4 reports
- AnchorFast Guard Select 9700Hollister Incorporated · DEVICE, FIXATION, TRACHEAL TUBE1 recall1 report
- 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.