Vital Signs™ A4Y580X4FRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752120242), received between Oct 30, 2024 and Oct 30, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Disconnection” (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. 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 30, 2024Disconnection; Disconnection

  FDA USER FACILITY MW REPORT MW 0500470000-2024-0039 REPORTED, THE CIRCUIT SEPARATED AT THE JOINT MULTIPLE TIMES DURING THE CASE, HAD TO INTERVENE. THE CIRCUIT DISCONNECTED MULTIPLE TIMES AT THE Y CONNECTION DURING THE CASE. CAUSED INTERRUPTION OF THE PROCEDURE AND INTERFERED WITH THE ANESTHESIA PATIENT CARE. THERE WAS NO REPORTED INJURY.

  Patient problems: Insufficient Information

  MAUDE report 20570960 ↗