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DRIVE 795RGRecalls & reported problems

Drive Devilbiss Healthcare · Rollators 4-Wheel Alum. Product Description Duet Rollator/TransportChair,Rose, 1/ea · 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 00822383000855), received between Mar 8, 2022 and Mar 8, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “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

  • Fracture1

Patient problems

  • Easy Bruising1
  • Fall1
  • Pain1

Recent adverse event reports

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

  • InjuryMar 8, 2022Fracture; Fracture

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT THAT OCCURRED ON (B)(6) 2021 INVOLVING A ROLLATOR/TRANSPORT CHAIR. THE END USER REPORTED THAT SHE WAS BEING TRANSPORTED IN THE DEVICE WHEN THE RIGHT WHEEL JAMMED AND FELL OFF, CAUSING HER TO SLIDE OFF OF THE DEVICE AND LAND ON HER KNEES. THE END USER REPORTED PAIN AND BRUISING IN BOTH KNEES, AS WELL AS A PULLED MUSCLE IN HER RIGHT SIDE AS A RESULT OF ATTEMPTING TO HOLD ONTO THE DEVICE TO AVOID FALLING. THE END USER ALSO REPORTED THAT SHE DID NOT GO TO THE HOSPITAL DUE TO COVID. DEVILBISS IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT TO INSPECT IT.

    Patient problems: Easy Bruising; Fall; Pain

    MAUDE report 13698443 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

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