Medline Industries, Inc. DYNJ66312Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489335729), received between Jul 14, 2022 and Jul 14, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 14, 2022Misfire; Defective Device

  WHEN DOCTOR ACTIVATED THE SKIN STAPLER, THE STAPLE MISFIRED AND DID NOT STAPLE. STAPLE IS POINTING OUT FROM STAPLER. DEFECTIVE STAPLER COLLECTED FROM STERILE FIELD AND A NEW SKIN STAPLER PRESENTED TO STERILE FIELD.

  Patient problems: Insufficient Information

  MAUDE report 15012462 ↗