Medline DYNJP2207SRecalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10884389103227), received between Sep 10, 2026 and Sep 28, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Material Integrity Problem” (3 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 28, 2026Fluid/Blood Leak

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50926672 ↗
• MalfunctionSep 28, 2026Fluid/Blood Leak

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50926657 ↗
• MalfunctionSep 25, 2026Material Integrity Problem

  Patient problems: Exposure to Body Fluids

  MAUDE report 50902867 ↗
• MalfunctionSep 18, 2026Material Integrity Problem

  It was reported that "Strike through of blood and fluids for long duration cases."

  Patient problems: Exposure to Body Fluids

  MAUDE report 50820077 ↗
• MalfunctionSep 10, 2026Material Integrity Problem

  Patient problems: Exposure to Body Fluids

  MAUDE report 50716712 ↗