Argyle 8888572560Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521025479), received between Jul 11, 2019 and Jul 11, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

• MalfunctionJul 11, 2019Break; Break

  THE CUSTOMER REPORTED THAT THE DRAIN USED IN THORACIC SURGERY BROKE AT ITS END WHEN PULLED FROM THE PLASTIC TUBE PACKAGE FOR USE IN THE PATIENT. THE DRAIN END REMAINED WITH THE CLAMP THAT WAS USED TO PULL IT OUT. THE HEALTH CARE PROVIDER USED ANOTHER DRAIN AND THERE WAS NO CONSEQUENCE TO THE PATIENT OR DELAY IN THE PROCEDURE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8781283 ↗