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Freedom 500 FM500 (UDI 00670482000463)Recalls & reported problems

Umano Medical Inc · Medical bed. · 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 00670482000463), received between Nov 7, 2021 and Nov 7, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Solder Joint Fracture” (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

  • Solder Joint Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionNov 7, 2021Solder Joint Fracture; Solder Joint Fracture

    DISTRIBUTOR CONTACTED TECHNICAL SERVICE OF MANUFACTURER TO REPORT ABOUT A BED WITH A BROKEN FOOT SIDERAIL ARM. HE MENTIONED THAT THE WELDING ON THE END OF THE LINK ARM WAS FOUND DEFECTIVE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12759119 ↗

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.