Go Go ES 2 3 Wheel S81Recalls & reported problems
Pride Mobility Products Corp · A motorized three-wheeled vehicle is a gasoline-fueled or battery-powered device intended for medical purposes that is used for outside transportation by disabled persons. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00606509300148), received between Mar 22, 2018 and Jun 18, 2025 — classified as 4 injuries, 1 malfunction.
The most frequently reported specific device problem is “Fire” (1 report).
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
- Fire1
Patient problems
- Bone Fracture(s)2
- Abrasion1
- Injury1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJun 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S DAUGHTER ALLEGES WHILE HER MOTHER WAS SHOPPING, THE STEERING WHEEL COLUMN ALLEGEDLY COLLAPSED ONTO HER LAP AND THE ACCELERATOR BUTTON PRESSED AGAINST HER LAP CAUSING THE UNIT TO STILL ACCELERATE ALLEGEDLY CAUSING HER MOM TO CRASH INTO A DISPLAY CASE.
Patient problems: Abrasion
MAUDE report 22282443 ↗InjuryJul 9, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S WIFE ALLEGES HE WAS TURNING INTO THE BEDROOM, THE BACK WHEEL CAUGHT THE DOOR, AND THE UNIT ALLEGEDLY TIPPED OVER WITH ARNOLD IN IT. HE BELIEVED HE WASN'T MAKING A TURN AT THAT MOMENT AND THAT IT WAS MORE OF A STRAIGHT AWAY AND DIDN'T CLEAR SUCCESSFULLY.
Patient problems: Bone Fracture(s)
MAUDE report 19700301 ↗InjuryNov 21, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS ATTEMPTING TO GO UP TO STEEP OF A RAMP AND ALLEGEDLY FLIPPED OFF.
Patient problems: Bone Fracture(s)
MAUDE report 18181166 ↗InjuryOct 24, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER WAS STRUCK BY A VEHICLE WHILE IN A CROSSWALK.
Patient problems: Injury
MAUDE report 9233946 ↗MalfunctionMar 22, 2018Fire; Fire
PROVIDER ALLEGES THE CONSUMER ALLEGES THE GAUGE ON HIS SCOOTER ALLEGEDLY CAUGHT FIRE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7360968 ↗
Other Vehicle, Motorized 3-Wheeled devices
- Go Go Elite Traveller 3 Wheel SC40E/Fun 3 WheelPride Mobility Products Corp · Vehicle, Motorized 3-Wheeled45 reports
- Victory 10 3 Wheel SC610/S610/ Colt Plus/Life HMV 3 Wheel/Beaufort 10/Pathrider 10 3 WheelPride Mobility Products Corp · Vehicle, Motorized 3-Wheeled17 reports
- Go Go Elite Traveller 4 Wheel SC44E/Fun 4 WheelPride Mobility Products Corp · Vehicle, Motorized 3-Wheeled15 reports
- Victory 10 4 Wheel SC710/S710/Life HMV 4 Wheel/Pathrider 10 4 WheelPride Mobility Products Corp · Vehicle, Motorized 3-Wheeled12 reports
- Travel Pro ES SC336Pride Mobility Products Corp · Vehicle, Motorized 3-Wheeled9 reports
- Go Go Sport 4 Wheel S74/Go Go ET Sport/Beaufort 6Pride Mobility Products Corp · Vehicle, Motorized 3-Wheeled8 reports
- Luna Victory SC613/S613/Eclipse/Luna Victory Economy/S613ECPride Mobility Products Corp · Vehicle, Motorized 3-Wheeled7 reports
- Drive SFPRO317FS-21Drive Devilbiss Healthcare · VEHICLE, MOTORIZED 3-WHEELED7 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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