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DRIVE RTL12032KDRRecalls & reported problems

Drive Devilbiss Healthcare · Bath Safety Transfer Product Description Splash Defense Transfer Bench · Class 1

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383001432), received between May 24, 2023 and May 24, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Misassembly by Users” (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

  • Misassembly by Users1

Patient problems

  • Fall1
  • Head Injury1

Recent adverse event reports

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

  • InjuryMay 24, 2023Misassembly by Users; Misassembly by Users

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A TRANSFER BENCH BY AN END USER'S MOTHER, WHO STATED THAT "THE CHAIR FELL BACKWARDS WHILE MY SON WAS SHOWERING. HE HIT HIS HEAD ON THE SHOWER WALL AS HE FELL BACKWARDS," REPORTEDLY CAUSING A "LUMP ON HIS HEAD." THERE WAS NO MEDICAL TREATMENT SOUGHT. UPON FOLLOW UP WITH THE END USER'S MOTHER, SHE REPORTED THAT "NOT ALL SUCTION CUPS WERE INSTALLED ON THE UNIT." THEY WERE LATER INSTALLED, AND SHE WILL CONTINUE TO USE THE UNIT. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

    Patient problems: Fall; Head Injury

    MAUDE report 16994666 ↗

Other ADAPTOR, HYGIENE devices

All ADAPTOR, HYGIENE devices →

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