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

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00670482000500), received between Oct 20, 2022 and Jan 15, 2025 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Communication or Transmission 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 15, 2025Defective Alarm; Improper or Incorrect Procedure or Method; Defective Alarm; Improper or Incorrect Procedure or Method

  ON (B)(6) 2024, A CUSTOMER REPORTED TO THE MANUFACTURER'S TECHNICAL SERVICE THAT THE BED EXIT MONITORING SYSTEM WAS TRIGGERING AN ALARM IMMEDIATELY UPON ARMING. THE SITE'S TECHNICIAN INITIATED TROUBLESHOOTING, BUT THE ISSUE REMAINED UNRESOLVED. TROUBLESHOOTING WAS SCHEDULED TO CONTINUE THE FOLLOWING DAY, AND THE MEDICAL STAFF CONTINUED TO USE THE DEVICE. ON (B)(6) 2024, DURING TROUBLESHOOTING, THE SITE'S TECHNICIAN INFORMED THE MANUFACTURER THAT A PATIENT HAD FALLEN FROM THE BED THE PREVIOUS NIGHT (EXACT DATE AND TIME NOT DISCLOSED). THE BED ACTIVITY LOG CONFIRMED THAT THE BED EXIT MONITORING SYSTEM WAS ACTIVATED AT 21:03 AND AN ALARM WAS TRIGGERED AT 8:41.

  Patient problems: Bruise/Contusion; Fall

  MAUDE report 21162327 ↗
• MalfunctionMar 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  CUSTOMER CALLED THE TECHNICAL SERVICE OF MANUFACTURER TO REPORT ABOUT A BED WITH TWO BROKEN BRAKE BARS. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18837556 ↗
• MalfunctionJun 27, 2023Communication or Transmission Problem; Communication or Transmission Problem

  THE MANUFACTURER WAS CONTACTED BY CUSTOMER ALLEGING THAT THE NURSE CALL SIGNAL WAS NOT BEING RECEIVED THROUGH THE NURSE CALL SYSTEM. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17209070 ↗
• MalfunctionDec 1, 2022Communication or Transmission Problem; Communication or Transmission Problem

  TECHNICAL SERVICE OF THE MANUFACTURER WAS INFORMED THAT THE BRAKE BED STATUS OF HOSPITAL BED WORKS INTERMITTENTLY. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15898175 ↗
• MalfunctionOct 20, 2022Electrical Shorting; Electrical Shorting

  CUSTOMER REPORTED TO UMANO REPRESENTATIVE THAT THE BED IS OVERLOADING THE NURSE CALL CIRCUIT BOARD MAKING IT NON FUNCTIONAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15638143 ↗
• MalfunctionOct 20, 2022Electrical Shorting; Electrical Shorting

  CUSTOMER REPORTED TO UMANO REPRESENTATIVE THAT THE BED IS OVERLOADING THE NURSE CALL CIRCUIT BOARD MAKING IT NON FUNCTIONAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15638017 ↗