Argyle 8888572552Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521025469), received between Oct 20, 2017 and Oct 20, 2017 — classified as 2 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. 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 20, 2017Break; Break

  THE CUSTOMER REPORTS THE TUBING OF THE CATHETER CONTINUED TO BREAK APART WHEN THE PHYSICIAN WENT TO USE IT. THEY HAD TO REPLACE THE PRODUCT.

  Patient problems: No Information

  MAUDE report 6965834 ↗
• MalfunctionOct 20, 2017Break; Break

  THE CUSTOMER REPORTS THE TUBING OF THE CATHETER CONTINUED TO BREAK APART WHEN THE PHYSICIAN WENT TO USE IT. THEY HAD TO REPLACE THE PRODUCT.

  Patient problems: No Information

  MAUDE report 6965736 ↗