Pulset 3302Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00709078011887), received between Aug 9, 2024 and Aug 9, 2024 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 9, 2024Break; Break

  WHEN PURGING AND REMOVING THE CAP THE TIP BROKE DOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19955614 ↗
• MalfunctionAug 9, 2024Break; Material Fragmentation; Break; Material Fragmentation

  THE NEEDLE WAS BROKEN COMPLETELY AT THE ARTERIAL PUNCTURE SITE WHEN REMOVING THE ABG.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19955510 ↗
• MalfunctionAug 9, 2024Fluid/Blood Leak; Infusion or Flow Problem; Fluid/Blood Leak; Infusion or Flow Problem

  SOME OF THE BLOOD OVERFLOWS FROM THE SYRINGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19955343 ↗