Medline Industries, Inc. DYNJ04058Recalls & reported problems
Medline Industries, Inc. · SKIN STAPLE REMOVER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10080196846924), received between Sep 17, 2026 and Sep 28, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (6 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
- Loose or Intermittent Connection6
- Material Too Soft/Flexible1
- Mechanical Problem1
- Unstable1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917960 ↗MalfunctionSep 28, 2026Loose or Intermittent Connection
It was reported that the staple remover Is not properly removing staples. The pin that connects the piece is loose.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915687 ↗MalfunctionSep 28, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50910503 ↗MalfunctionSep 25, 2026Unstable; Material Too Soft/Flexible
It was reported that "the point seems smaller and flimsy. It does not work for removing regular skin staples as it is too small."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50899290 ↗MalfunctionSep 23, 2026Loose or Intermittent Connection
It was reported that the staple remover Is not properly removing staples. The pin that connects the piece is loose.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872986 ↗MalfunctionSep 21, 2026Mechanical Problem
It was reported that "THEY HAVE BEEN HAVING ISSUES WITH THE STAPLE REMOVER, MOST OF THE TIME IT BREAKS THE STAPLE WITHOUT MOVING IT AND DOES NOT REMOVE THE STAPLES."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50840357 ↗MalfunctionSep 18, 2026Loose or Intermittent Connection
It was reported that "Staff are reporting the medline have a very loose joint and causes the staple to slip around not allowing a nice pinch to remove the staple. The staples are bending weird causing increased pain to the patients. Bending weird can cause the staples to go into the skin or a difficult removal."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50818330 ↗MalfunctionSep 17, 2026Loose or Intermittent Connection
It was reported that the staple remover Is not properly removing staples. The pin that connects the piece is loose.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50797298 ↗
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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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