Medline Industries, Inc. DYNJ03108LFRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10080196841202), received between Aug 31, 2026 and Sep 22, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Unsealed Device Packaging” (2 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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2026Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging

  It was reported that "Protective covering/packaging is prematurely tearing open."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50853707 ↗
• MalfunctionSep 15, 2026Crack

  It was reported that "As soon as the provider tried to suture with the forceps the suture needle kept falling out." It was also reported that "It looks like a crack going through" and "when they close the ratchet the jaws do not always close completely."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50778307 ↗
• MalfunctionSep 1, 2026Unsealed Device Packaging

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50550191 ↗
• MalfunctionAug 31, 2026Material Puncture/Hole

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50519972 ↗