Medline FCE1232BLRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 40884389117270), received between Aug 7, 2026 and Sep 18, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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.

• MalfunctionSep 18, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50831077 ↗
• MalfunctionAug 7, 2026Electrical /Electronic Property Problem

  It was reported that the head of the bed will not raise or lower. It was reported that the bed will not go down when he presses the down button for the high low function and the T cable will not work on one side.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50181561 ↗