Jazzy EVO 613 LI JZEVO613LIRecalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00606509100274), received between Jun 16, 2023 and Feb 16, 2026 — classified as 2 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 Available2
Patient problems
- Bone Fracture(s)1
- Burn(s)1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 16, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES ONE DAY THE CHAIR STOPPED HIS PHONE FELL ON THE FLOOR AND WHEN HE DROPPED THE PHONE HE TRIED TO BEND OVER TO PICK THE PHONE UP AND HE FELL OUT OF THE CHAIR AND ALLEGEDLY BROKE HIS ANKLE. CONSUMER ALSO ALLEGES HE HAS BEEN STRANDED 7 TIMES WHERE HE WILL BE USING THE PRODUCT FOR 10-20 MINUTES AND THE EVO ALLEGEDLY JUST SHUTS OFF NO POWER AND HE IS STUCK. HE ALLEGED HE HAD TO CALL 911 MORE THAN ONCE.
Patient problems: Bone Fracture(s)
MAUDE report 24344060 ↗InjuryJun 16, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER ALLEGES THE UNIT STOPPED AND WOULD NOT GO BACK ON FOR ONE OCCASION. THE CONSUMER ALSO ALLEGES ANOTHER TIME IT STOPPED, HE SHUT IT OFF AND THEN IS STARTED BUT ALLEGEDLY STOPPED AGAIN.
Patient problems: Burn(s)
MAUDE report 17142233 ↗
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- 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.
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