MEDLINE DYNJ04058ARecalls & reported problems
Medline Industries, Inc. · SKIN STAPLE REMOVER · Class 1
- 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 10653160385769), received between Aug 12, 2026 and Sep 14, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Difficult to Open or Close1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Break; Mechanical Jam
It was reported that "the problem is that the new item when the nurse/doctor have tried to remove the staple it locks and is a patient safety."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50756905 ↗MalfunctionAug 12, 2026Difficult to Open or Close
Patient problems: Pain
MAUDE report 50228845 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.