39 Low Boy Bed LO39Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00845699000012), received between Jun 3, 2025 and Jun 4, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Use of Device 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 16, 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.

• MalfunctionJun 4, 2025Use of Device Problem; Use of Device Problem

  BEDFRAME NOT WORKING PROPERLY WHILE IN PATIENT USE, HOWEVER PATIENT WAS NOT INJURED. BED'S HEAD ARTICULATION HAS MOVEMENT BUT IS JERKY. PATIENT NEEDS TO HELP THE ACTUATOR IN ORDER FOR IT TO MOVE. ACTUATOR GIVES OUT WHEN PUTTING A LOAD OF WEIGHT ON IT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22146502 ↗
• MalfunctionJun 3, 2025Use of Device Problem; Use of Device Problem

  ORIGINAL SUBMISSION ON 4/7/2025 STATES BED'S ECM IS NOT WORKING PROPERLY. BED'S UP/DOWN ACTUATORS AND FOOT ARTICULATION ACTUATORS ARE NOT MOVING. BED'S HEAD ARTICULATION HAS MOVEMENT BUT IS JERKY. BED'S UP/DOWN ACTUATORS MOVE IF PLUGGED INTO HEAD ARTICULATION PORT. ON 5/28/2025 LEARNED OF PATIENT INVOLVEMENT WITHOUT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22137702 ↗