MAUDE Adverse Event Report: UNKNOWN SCOOTER MIDSIZE 3 WHEEL SILVER 9153652403; VEHICLE, MOTORIZED 3-WHEELED

Model Number SCOOTERS

Device Problems Electrical /Electronic Property Problem (1198); Sparking (2595); Battery Problem (2885)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Type  malfunction  

Manufacturer Narrative

A follow up will be sent if the product or additional information is obtained.

Event Description

The dealer spoke with tech services.The dealer put new batteries in the box and the hooked the wiring up.The battery sparked and popped the breaker in the battery box.

• Brand Name: SCOOTER MIDSIZE 3 WHEEL SILVER 9153652403
• Type of Device: VEHICLE, MOTORIZED 3-WHEELED
• Manufacturer (Section D): UNKNOWN; OH
• Manufacturer (Section G): UNKNOWN; OH
• Manufacturer Contact: kevin guyton ; one invacare way; elyria, OH 44035 ; 8003336900
• MDR Report Key: 4992655
• MDR Text Key: 23950148
• Report Number: 1525712-2015-04220
• Device Sequence Number: 1
• Product Code: INI
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor
• Reporter Occupation: Medical Equipment Company Technician/Representative
• Report Date: 07/17/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/11/2015
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: SCOOTERS
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 07/17/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1
• Patient Outcome(s): Other