Medline Industries, Inc. DYNJ04059Recalls & reported problems
Medline Industries, Inc. · SKIN STAPLE REMOVER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10884389398487), received between May 1, 2026 and Sep 22, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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
- Insufficient Device Problem Information1
- Mechanical Problem1
Patient problems
- Discomfort1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Mechanical Problem
It was reported that the prongs went under the staple, but the top prong would not catch the staple to remove.
Patient problems: Discomfort
MAUDE report 50858317 ↗MalfunctionMay 1, 2026Insufficient Device Problem Information
ACCORDING TO THE FACILITY, THE STAPLER REMOVER THEY HAVE IS "NOT A GOOD ONE." THEY HAVE A HARD TIME CUTTING THE STAPLES OFF THE PATIENTS. THE PATIENT WAS COMPLAINING HOW IT WAS PAINFUL WHEN THEY WERE TRYING TO REMOVE THE STAPLES BECAUSE IT KIND OF CUT INTO THE WOUND. THE FACILITY STATED IT DOES NOT WORK PROPERLY.
Patient problems: Pain
MAUDE report 25059552 ↗
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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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