Medline Industries, Inc. DYNJ07254ARecalls & reported problems
Medline Industries, Inc. · SUTURE REMOVAL TRAY · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10080196039654), received between Mar 30, 2026 and Sep 29, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Corroded” (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. 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
- Corroded2
- Dull, Blunt1
- Failure to Align1
- Failure to Cut1
- Material Separation1
- Mechanical Problem1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937133 ↗MalfunctionSep 28, 2026Peeled/Delaminated
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917174 ↗MalfunctionSep 24, 2026Mechanical Problem; Failure to Align; Failure to Cut
It was reported that "gauze are light weight and blow off the patient," "gauze get wet, stick to the patient and tear easily," "scissors are difficult to use and have to use more force to get them to cut," "scissors are not lined up correctly," and "needle holders will not hold sutures well."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50887217 ↗MalfunctionSep 22, 2026Material Separation
It was reported that "today I was using a pair of scissors in the suture removal kit and they broke apart into 2 different pieces in my hands".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854338 ↗MalfunctionMar 31, 2026Corroded
RUST ON COMPONENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24737948 ↗MalfunctionMar 30, 2026Corroded
RUST ON COMPONENT IN PACKAGING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24737312 ↗
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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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