Medline Industries, Inc. DYNJ64242BRecalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10193489956405), received between Sep 9, 2026 and Sep 28, 2026 — classified as 9 malfunctions.

The most frequently reported specific device problem is “Packaging Problem” (9 reports).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Apr 21, 2023Class IIOpen, Classified

   The kits were damaged by water.

   Z-1646-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 28, 2026Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50924099 ↗
• MalfunctionSep 25, 2026Packaging Problem

  It was reported that "We returned several custom packs a few weeks ago because they arrived soaking wet. Evidently they were repackaged and sent back to us for use."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50897611 ↗
• MalfunctionSep 22, 2026Packaging Problem

  It was reported that "Wet packs potentially used on patient."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50854195 ↗
• MalfunctionSep 15, 2026Packaging Problem

  It was reported that Wet packs potentially used on patient.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50773856 ↗
• MalfunctionSep 15, 2026Moisture Damage; Packaging Problem

  It was reported that "Wet packs potentially used on patient."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50773269 ↗
• MalfunctionSep 14, 2026Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50763735 ↗
• MalfunctionSep 10, 2026Packaging Problem

  It was reported that "Wet packs potentially used on patient."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50714665 ↗
• MalfunctionSep 9, 2026Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50698764 ↗
• MalfunctionSep 9, 2026Packaging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50698596 ↗