Drive RTL10266CH-HSRecalls & reported problems
Drive Devilbiss Healthcare · Nitro,FirmFoam,ChampagneFrame,RTL 1/ea · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822383549477), received between Feb 25, 2025 and Sep 2, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Mechanical Problem” (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.
Reports received per month
Most reported problems
Device problems
- Mechanical Problem1
- Structural Problem1
Patient problems
- Blister1
- Bone Fracture(s)1
- Limb Fracture1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 2, 2026Mechanical Problem
Patient problems: Blister; Limb Fracture
MAUDE report 50569323 ↗InjuryFeb 25, 2025Structural Problem; Structural Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER, WHO STATED THAT A WHEEL ON THE ROLLATOR BENT WHILE IN USE CAUSING HER TO FALL AND BREAK HER LEFT ANKLE AND TIBIA. THE END USER IS NOT RETURNING THE DEVICE FOR EVALUATION. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.
Patient problems: Bone Fracture(s)
MAUDE report 21459788 ↗
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- Drive R726BKDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
- Drive R728BLDrive Devilbiss Healthcare · WALKER, MECHANICAL9 reports
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- Drive RTL10266Drive Devilbiss Healthcare · WALKER, MECHANICAL8 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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