Merit Medical® 00884450349038Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884450349038), received between Mar 25, 2020 and Mar 25, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (1 report).

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. Jun 11, 2024Class IIOpen, Classified

   Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

   Z-2579-2024 · Root cause: No Marketing Application · Recall details · FDA record ↗

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.

• InjuryMar 25, 2020Fracture; Material Fragmentation; Fracture; Material Fragmentation

  THE ACCOUNT ALLEGES THAT DURING AN INTRAVASCULAR PROCEDURE, A GUIDEWIRE TIP DETACHED WITHIN THE PATIENT'S ARTERY. THE CLINICIAN WAS SUCCESSFUL IN REMOVING THE FOREIGN BODY WITH A VASCULAR SNARE DEVICE. NO PATIENT INJURY TO REPORT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9881122 ↗