MAUDE Adverse Event Report: Pride Mobility Products Corporation Pride Mobility Products; Vehicle, Motorized 3-Wheeled

Model Number	Go Go Endurance AL+ (SC54ALX)
Medical Device Problem Code	Appropriate Device Problem Term/Code Not Available (3191)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/17/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The provider alleges the consumer alleges they charged the unit overnight and disconnected from the charger, put the battery pack, on the scooter, put it in drive, put the key in the ignition, turned it on the battery pack allegedly caught fire sparked and smoked.
Additional Manufacturer Narrative
The device has not yet been made available for evaluation.Should further information or the device become available, a follow-up report will then be issued.
Event or Problem Description
The provider alleges the consumer alleges they charged the unit overnight and disconnected from the charger, put the battery pack, on the scooter, put it in drive, put the key in the ignition, turned it on the battery pack allegedly caught fire sparked and smoked.
Additional Manufacturer Narrative
Upon inspection, it was determined that no fire occurred at the output pins of the battery terminals.Measurements taken at the receiving side of the battery red+ and black- terminals confirmed a short circuit between the pins on the unit side.Further investigation traced the short circuit to the tiller harness.An assembly mounting screw had been driven through the harness during the assembly, causing damage to the wiring and creating a direct short.This condition resulted in the thermal event at the battery terminal output pins when battery was placed on unit.

• Brand Name: Pride Mobility Products
• Common Device Name: Vehicle, Motorized 3-Wheeled
• Manufacturer (Section D): Pride Mobility Products Corporation; 401 york avenue; duryea PA 18643
• Manufacturer (Section G): N/A; n/a; n/a; n/a
• Manufacturer Contact: kelly livingston ; 401 york avenue; duryea, PA 18643 ; +1(800)800-8586
• MDR Report Key: 50081571
• Report Number: 2530130-2026-01371
• Device Sequence Number: 10253060
• Product Code: INI
• UDI-Device Identifier: 00606509300858
• UDI-Public: 00606509300858
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K063389
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/01/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: Go Go Endurance AL+ (SC54ALX)
• Device Catalogue Number: N/A
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 08/17/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/20/2026
• Supplement Date Received by Manufacturer: 07/20/2026
• Initial Report FDA Received Date: 07/30/2026
• Supplement Report FDA Received Date: 10/01/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/08/2025
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown