Jazzy SelectRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509100120), received between Nov 22, 2021 and Jan 29, 2026 — 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.

• InjuryJan 29, 2026Appropriate Device Problem Term/Code Not Available

  CARETAKER ALLEGES THE CONSUMER WAS DRIVING HER SCOOTER AND WAS STRUCK BY A VEHICLE. CONSUMER WAS THEN DRAGGED BY SAID VEHICLE FOR 10 FEET.

  Patient problems: Abrasion

  MAUDE report 24210844 ↗
• InjuryJan 12, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES WHEN SHE WENT TO PUT THE FOOTPLATE DOWN, IT'S ALLEGEDLY SO HEAVY THAT IS SCRAPPED HER LEG.

  Patient problems: Laceration(s)

  MAUDE report 16148082 ↗
• InjuryAug 2, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES SHE WAS RIDING IN HER CHAIR WHEN THE BACK ALLEGEDLY CAME OFF ALLEGEDLY CAUSING HER TO FALL OUT OF THE CHAIR.

  Patient problems: Bruise/Contusion

  MAUDE report 15145060 ↗
• InjuryNov 22, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES HE WAS GOING UP A RAMP TO HIS HOUSE WHEN HIS CHAIR ALLEGEDLY TIPPED BACKWARDS AND LANDED ON HIM.

  Patient problems: Bruise/Contusion

  MAUDE report 12851796 ↗