Jazzy EVO 613 JZEVO613Recalls & reported problems
Pride Mobility Products Corp · A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509100281), received between Aug 24, 2023 and Oct 3, 2024 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available4
Patient problems
- Abrasion1
- Bone Fracture(s)1
- Damage to Ligament(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryOct 3, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HIT A BLIND SPOT AND RAN INTO A CURB AND THE UNIT ALLEGEDLY FLIPPED ON TOP OF HIM.
Patient problems: Damage to Ligament(s)
MAUDE report 20358998 ↗InjuryJun 26, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S SON ALLEGES HIS MOM WHILE RESTING HER FEET ON THE FLOOR SHE ACCIDENTALLY REACHES FOR SOMETHING AND HER SLEEVE CATCHES THE JOY STICK, THE CHAIR WILL ALLEGEDLY ACTIVATE, STARTS GOING IN CIRCLES AND ALLEGEDLY THROWS HER OFF OF IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19616776 ↗InjurySep 29, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES HE GOT HIS FOOT CAUGHT SOMEWHERE UNDER THE FOOTPLATE.
Patient problems: Bone Fracture(s)
MAUDE report 17842383 ↗InjuryAug 24, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THAT HE HAS BEEN WAITING FOR NEW ELR'S. THE CONSUMER HAS A SINGLE RIGHT LEG AMPUTATION AND ALSO HAS SEVERE EDEMA. HE IS ALLEGING THAT FROM NOT HAVING THE ELR'S HE ALLEGEDLY HAS SWELLING, BLISTERS AND NOW ABSCESSES.
Patient problems: Abrasion
MAUDE report 17611633 ↗
Other Wheelchair, Powered devices
- SmartDrive® MX2+Max Mobility, LLC · Wheelchair, Powered858 reports
- Permobil M3Permobil, Inc. · Wheelchair, Powered1 recall59 reports
- TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGInvacare Corporation · Wheelchair, powered2 recalls2 reports
- TDX SP2 with LiNX Electronics TDXSP2Invacare Corporation · Wheelchair, powered2 recalls0 reports
- Invacare® TDX SP2 with Captain's Seat TDXSP2VInvacare Corporation · Wheelchair, powered2 recalls0 reports
- Q6 Edge 3Pride Mobility Products Corp · Wheelchair, Powered4 deaths86 reports
- Q6 Edge 2.0 Q6 Edge 2.0 / Q6 Edge 2.0 with iLevelPride Mobility Products Corp · Wheelchair, Powered1 death83 reports
- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page