Jazzy Carbon HDRecalls & 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
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00606509100397), received between May 11, 2026 and Jun 29, 2026 — classified as 6 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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available6
Patient problems
- Bone Fracture(s)2
- Bruise/Contusion2
- Damage to Ligament(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryJun 29, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER'S HUSBAND ALLEGES UNIT TIPPED FORWARD CAUSING HIS WIFE (B)(6) TO HIT HER HEAD.
Patient problems: Bruise/Contusion
MAUDE report 25650136 ↗InjuryJun 4, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER'S WIFE ALLEGES AT THE AIRPORT WHILE CROSSING A THRESHOLD THE CHAIR ALLEGEDLY CAME TO A COMPLETE STOP AND THREW HER HUSBAND FROM THE CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 25392212 ↗InjuryJun 4, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS GOING UP A MINIMAL INCLINE WHEN THE CHAIR ALLEGEDLY TIPPED FORWARD AND THE CONSUMER FELL OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25392211 ↗InjuryMay 29, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER'S HUSBAND ALLEGES THAT HIS WIFE'S CHAIR TIPPED OVER WITH HER IN IT.
Patient problems: Bone Fracture(s)
MAUDE report 25330111 ↗InjuryMay 14, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HIS UNIT BUCKED HIM AND HE ALLEGEDLY FELL ON FLOOR. HE ALSO ALLEGES THE PRODUCT FELL ON TOP OF HIM.
Patient problems: Bruise/Contusion
MAUDE report 25171431 ↗InjuryMay 11, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS DRIVING CHAIR INSIDE SENIOR LIVING FACILITY WHEN FRONT CASTER ARM ALLEGEDLY CAME APART AND USER FELL OUT OF UNIT.
Patient problems: Damage to Ligament(s)
MAUDE report 25134656 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.