MyOn™ Active Wheelchair MYONACRecalls & reported problems
Invacare Corporation · MyOn™ Active Wheelchair · Class 1
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 00841447102304), received between Nov 26, 2024 and Dec 13, 2024 — 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)2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 13, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED WHEN A USER WAS TRANSFERRING FROM THE ACTION 3NG WHEELCHAIR TO THE TOILET, THE USER HAD DROPPED FROM THE WHEELCHAIR BETWEEN THE TOILET SEAT AND WHEELCHAIR. THE USER COULD NOT GET UP BY HIMSELF. THE DOOR WAS CLOSED, AND THE PHONE WAS IN THE KITCHEN. THE USER TRIED TO OPEN THE DOOR BY KICKING IT BUT HIT HIS LITTLE TOE ON THE WHEELCHAIR´S FOOTREST TUBE. THERE WERE NO FOOTRESTS ATTACHED. THE LITTLE TOE SUSTAINED AN OPEN FRACTURE AS A RESULT OF THE IMPACT AND WAS AMPUTATED.
Patient problems: Bone Fracture(s)
MAUDE report 20926467 ↗InjuryNov 26, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THE PATIENT FELL OUT OF THE ACTION 4 NG WHEELCHAIR ON (B)(6)2024 AROUND 2PM. SHE WAS OUT WITH 2 OF HER CAREGIVERS WHO WERE PUSHING HER OUTSIDE. SHE WAS NOT WEARING HER LAP BELT. WHEN THEY TRIED TO GO UP ON TO THE PAVEMENT, THE CASTERS WERE NOT HIGH ENOUGH AND HIT THE CURB. SHE FELL FORWARDS OUT OF THE WHEELCHAIR AND FRACTURED HER KNEE AND SUSTAINED SOME SUPERFICIAL INJURIES TO HER ARMS AND FACE. SHE WAS TAKEN TO THE HOSPITAL WHERE SHE WAS TREATED. THE LEFT LEG IS NOW IN A CAST. THE OT REPORTER ADVISED THE PATIENT WILL NEED SURGERY TO HER KNEE.
Patient problems: Bone Fracture(s)
MAUDE report 20778097 ↗
Other Wheelchair, mechanical devices
- MEDLINE K1186N22SMedline Industries, Inc. · Wheelchair, mechanical48 reports
- Guardian K4186N24EMedline Industries, Inc. · Wheelchair, mechanical22 reports
- MEDLINE INDUSTRIES, INC. MDS808650Medline Industries, Inc. · Wheelchair, mechanical18 reports
- Medline MDS806850Medline Industries, Inc. · Wheelchair, mechanical17 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 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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