ook snow FL36 ook snow (REF FL36)Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00670482000593), received between May 18, 2023 and Sep 1, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Communication or Transmission Problem” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 1, 2026Electrical /Electronic Property Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50547762 ↗
• MalfunctionJul 28, 2026

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50054216 ↗
• MalfunctionDec 9, 2025Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THAT THE CASTER BRAKE OF AN HOSPITAL BED WAS ALLEGEDLY NOT STAYING IN LOCKED POSITION. THERE WAS NO PATIENT REPORTED TO BE INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23761425 ↗
• MalfunctionSep 11, 2024Communication or Transmission Problem; Communication or Transmission Problem

  THE CUSTOMER REPORTED TO UMANO MEDICAL REPRESENTATIVE THAT THE NURSE CALL SIGNAL IS NOT SENT FROM THE BED TO THE NURSE CALL SYSTEM. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20189552 ↗
• MalfunctionMay 18, 2023Component Misassembled; Component Misassembled

  CUSTOMER CONTACTED UMANO REPRESENTATIVE TO REPORT A PATIENT FALL WITHOUT INJURY. HE MENTIONED THAT THE EVENT OCCURED DUE TO A TILTED BED.

  Patient problems: Fall

  MAUDE report 16953036 ↗