Jazzy Select EliteRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509100151), received between Jul 15, 2019 and Feb 5, 2020 — classified as 4 injuries.

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 5, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  TECH WAS AT CONSUMER'S FOR A PREVIOUS ISSUE WHEN CONSUMER TOLD TECH THAT HIS CHAIR ALLEGEDLY TIPPED BACKWARDS WHILE GOING UP A STEEP RAMP.

  Patient problems: Injury

  MAUDE report 9670517 ↗
• InjuryFeb 5, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES SHE WAS CROSSING THE STREET WHEN A CAR TURNED INTO THE RIGHT SIDE OF HER DEVICE AND HIT HER.

  Patient problems: Pain

  MAUDE report 9670505 ↗
• InjuryAug 6, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES RELEASING THE JOYSTICK AND THE POWERCHAIR KEPT GOING AND CUSTOMER CRASHED INTO STOVE CAUSING INJURY.

  Patient problems: Injury

  MAUDE report 8864364 ↗
• InjuryJul 15, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES THAT THE CONTROLLER IS STICKING AND CAUSED CONSUMER TO RUN INTO STOVE CAUSING INJURY.

  Patient problems: Injury

  MAUDE report 8789663 ↗