Medline Industries, Inc. DYND07603Recalls & reported problems
Medline Industries, Inc. · CHEST TUBE TRAY · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884389257487), received between Sep 24, 2021 and Sep 30, 2026 — classified as 2 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Break” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
- Corroded1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Break
It was reported that Hemostat froke in half inserting a chest tube.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946560 ↗MalfunctionSep 28, 2026Corroded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923733 ↗InjurySep 24, 2021Break
IT WAS REPORTED THAT THE DISTAL JAW OF THE PEON COMPONENT BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12526110 ↗InjurySep 24, 2021Break
IT WAS REPORTED THAT THE DISTAL JAW OF THE PEON COMPONENT BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12525989 ↗
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- Medline Industries, Inc. DYNJ69692Medline Industries, Inc. · General surgery tray4 recalls0 reports
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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