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Freedom 500 FM500 (UDI 00670482000081)Recalls & reported problems

Umano Medical Inc · The Freedom500 is an AC-powered medical bed with 4 built-in electric DC actuators. The height and surface contours are adjustable. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00670482000081), received between Dec 20, 2017 and Dec 20, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

Device problems

  • Component Missing1
  • Device Misassembled During Manufacturing /Shipping1
  • Out-Of-Box Failure1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 20, 2017Component Missing; Out-Of-Box Failure; Device Misassembled During Manufacturing /Shipping; Component Missing; Out-Of-Box Failure; Device Misassembled During Manufacturing /Shipping

    IT WAS ALLEGED THAT A BED MODEL FM500 WAS FOUND WITH A SUPPORT ARM DISASSEMBLED FROM A FOOTEND RAIL. THE BED WAS NOT IN SERVICE, THE SITUATION WAS NOTICED DURING INSPECTION OF BED. THERE WERE NO REPORTED ADVERSE EVENT.

    Patient problems: No Patient Involvement

    MAUDE report 7133521 ↗

Other Bed, Ac-Powered Adjustable Hospital devices

All Bed, Ac-Powered Adjustable Hospital devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.