Jazzy AirRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509100069), received between Jan 10, 2018 and Jan 15, 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.

• InjuryJan 15, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES THAT CONSUMER WAS MOVING THROUGHOUT HER HOME WHEN THE CHAIR ALLEGEDLY SPED UP AND THEN SUDDENLY STOPPED ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT.

  Patient problems: Injury

  MAUDE report 9590313 ↗
• InjuryDec 13, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES CUSTOMERS FEET DO NOT FIT ON THE FOOT REST AND THEREFORE KEEPS CRASHING INTO THE WALLS.

  Patient problems: Bone Fracture(s)

  MAUDE report 8161209 ↗
• InjuryJul 18, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES COMING INTO APARTMENT AND USED LEG TO HOLD DOOR. WHILE HOLDING DOOR OPEN, USED ARM TO HIT THE JOYSTICK AND IT LURCHED FAST. DID NOT HAVE SEAT BELT ON. CUSTOMER FELL ON KNEE AND BROKE HER LEG.

  Patient problems: Bone Fracture(s)

  MAUDE report 7697839 ↗
• InjuryJan 10, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES SITTING IN CHAIR WHEN THE BOLTS ON THE ARMREST BROKE AND CUSTOMER FELL OUT OF CHAIR.

  Patient problems: Abrasion

  MAUDE report 7177817 ↗