MEDLINE 401904RHRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888277407602), received between Sep 23, 2026 and Sep 23, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Communication or Transmission Problem” (1 report).

3 FDA recall records name this device's identifier, 3 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. Dec 22, 2025Class IOpen, Classified

   These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

   Z-1321-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Jul 31, 2025Class IOpen, Classified

   Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.

   Z-2610-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

3. Feb 6, 2025Class IIOpen, Classified

   Devices may have higher than expected amounts of bacterial endotoxin.

   Z-1460-2025 · Root cause: Under Investigation by firm · 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.

• MalfunctionSep 23, 2026Communication or Transmission Problem

  It was reported that "Plugged in and wasn¿t receiving signal from certain pins."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50873050 ↗