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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00670482000685), received between Mar 27, 2025 and Apr 7, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Arcing” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 7, 2026Arcing; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE CABLE OF A HOSPITAL BED WAS ALLEGEDLY EMITTING SMOKE. NO INJURIES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24806319 ↗
• InjuryMar 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON FEBRUARY 25, 2025, CUSTOMER REPORTED TO UMANO MEDICAL'S TECHNICAL SERVICE THAT A PATIENT WAS FOUND WITH THEIR FOOT ENTRAPPED BETWEEN THE BOLSTER AND THE FOOTBOARD OF THE BED, RESULTING IN A TOE FRACTURE AND LACERATION. HE MENTIONED THAT THE BED IS EQUIPPED WITH AN MDF(WOOD) FOOTBOARD. ON FEBRUARY 27, 2025, UMANO WAS NOTIFIED BY ITS US AGENT OF THE VOLUNTARY MEDICAL DEVICE REPORT (MDR) NUMBER MW5162038 RELATED TO THE SAME COMPLAINT.

  Patient problems: Bone Fracture(s); Laceration(s)

  MAUDE report 21706504 ↗