Hoveround Teknique XHDRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00859781000033), received between Aug 14, 2019 and Mar 31, 2020 — classified as 3 injuries.

The most frequently reported specific device problem is “Use of Device Problem” (3 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 31, 2020Use of Device Problem; Use of Device Problem

  THE END USER WAS OPERATING THE POWER WHEELCHAIR WHILE IMPAIRED ON SLEEPING MEDICATION AND RAN INTO A WALL.

  Patient problems: Injury

  MAUDE report 9903384 ↗
• InjuryMar 9, 2020Use of Device Problem; Use of Device Problem

  THE END USER WAS OPERATING THE POWER WHEELCHAIR AT NIGHT IN A CROSSWALK AND WAS STRUCK BY A MOTOR VEHICLE.

  Patient problems: Injury

  MAUDE report 9805395 ↗
• InjuryAug 14, 2019Use of Device Problem; Use of Device Problem

  WHILE SITTING STATIONARY IN THE POWER WHEELCHAIR AND NOT WEARING A SEAT BELT, THE END USER SLID OUT ONTO THE FLOOR.

  Patient problems: Fall; Injury

  MAUDE report 8893778 ↗