MEDLINE DYNDBCHLDRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888277415461), received between Sep 29, 2026 and Sep 29, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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. How this data works · Data updated Oct 13, 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.

• MalfunctionSep 29, 2026Fluid/Blood Leak

  It was reported that "The hub is narrower, the rubber sheath on the needle does not fully retract when placed in the hub and on occasion the tube is not easily removed from the needle. In the picture below, the cap remained on the needle resulting in loss of blood" and "blood splatter is being left on the caps."

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 50931738 ↗