DRIVEMEDICAL RTLFW19RW-RDRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383246277), received between May 6, 2020 and Dec 29, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Collapse” (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 18, 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.

• InjuryDec 29, 2021Collapse; Collapse

  ACCORDING TO THE REPORT RECEIVED, THE END USER SUSTAINED "A HEAD INJURY" WHILE USING A TRANSPORT CHAIR AFTER THE BACK REST ON THE "DEVICE COLLAPSED" AND CAUSED THEM TO FALL. THE END USER RECEIVED UNSPECIFIED TREATMENT IN THE EMERGENCY ROOM. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE AS SOON AS ADDITIONAL INFORMATION BECOMES AVAILABLE.

  Patient problems: Head Injury

  MAUDE report 13112777 ↗
• InjuryMay 6, 2020Fracture; Fracture

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. WE HAVE NOT RECEIVED THE DEVICE YET FOR EVALUSTION. WE ARE FILING THIS REPORT IN AN OVER ABUNDANCE OF CAUTION. THE END USER WAS BEING PUSHED IN THE DEVICE FROM THE HALLWAY TO THE KITCHEN WHEN THE HANDLES BROKE CAUSING HER TO FALL.  SHE HIT HER HEAD BUT DID NOT SEEK MEDICAL ATTENTION.

  Patient problems: Fall

  MAUDE report 10028390 ↗