Medline Industries, Inc. DYNJ82937Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327224868), received between Sep 11, 2026 and Sep 17, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Corroded” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 17, 2026Corroded

  It was reported that there were "rusty instruments".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50804393 ↗
• OtherSep 11, 2026Tear, Rip or Hole in Device Packaging

  It was reported that "The units have wasted 4 packs so far because the packs are stuck on the tape that is supposed to secure the bottom of the boxes. When they pull them out, the packs are getting damaged and are no longer sterile."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50734985 ↗