DRIVEMEDICAL RTL12031KDRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50822383532887), received between Apr 13, 2020 and Apr 13, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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. 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 13, 2020Material Fragmentation; Material Fragmentation

  DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A BATH BENCH. THE DEVICE HAS NOT YET BEEN RETURNED FOR EVALUATION. IN AN OVERABUNDANCE OF CAUTION WE ARE FILING THIS REPORT SINCE THE END USER HIT THERI HEAD. WE WILL AMEND THE REPORT IF ANY ADDITIONAL DATA IS RECEIVED. THE PIN RUSTED ON THE CHAIR CAUSING THE SEAT TO COLLAPSE WHILE IN USE. ENDUSER FELL AND HIT HIS HEAD AND BRUISED HIS BACK. HE DID NOT SEEK MEDICAL ATTENTION.

  Patient problems: Fall

  MAUDE report 9955424 ↗