drive RTL799Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383006277), received between May 29, 2025 and May 29, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

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

• InjuryMay 29, 2025Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A KNEE WALKER BY THE END USER'S MOTHER WHO REPORTED THAT DURING USE, THE KNEE REST BROKE IN HALF FROM FRONT TO BACK CAUSING THE END USER TO FALL ON THE TOES OF HIS PRE-EXISTING INJURED FOOT. AN ULTRASOUND WAS PERFORMED REVEALING A SMALL BLOOD CLOT ALTHOUGH IT IS UNCERTAIN IF THIS WAS CAUSED BY THE FALL. THE DEVICE WAS RETURNED TO THE ORIGINAL RETAILER AND THEREFORE IS UNAVAILABLE FOR EVALUATION.

  Patient problems: Thrombosis/Thrombus

  MAUDE report 22107578 ↗