MAUDE Adverse Event Report: SUNRISE MEDICAL (US) LLC QUICKIE Q700M; WHEELCHAIR, POWERED

Device Problems Premature Discharge of Battery (1057); Device Emits Odor (1425); Overheating of Device (1437); Defective Component (2292); Battery Problem (2885)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Type  malfunction  

Event Description

Chair has left me stranded; since delivery on (b)(6) 2020 the chair cannot hold a proper charge.They replaced the batteries at least three times.Three weeks ago they finally replaced the motors.Now the motor overheats and smells of burned oil.They stated the motor is safe to reach '250* f'.Skin burns at '118* f' there are no guards in place.Fda safety report id# (b)(4).

• Brand Name: QUICKIE Q700M
• Type of Device: WHEELCHAIR, POWERED
• Manufacturer (Section D): SUNRISE MEDICAL (US) LLC
• MDR Report Key: 12331775
• MDR Text Key: 267220005
• Report Number: MW5103292
• Device Sequence Number: 1
• Product Code: ITI
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 08/13/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/16/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Was Device Available for Evaluation?: Yes
• Was Device Evaluated by Manufacturer?: No Information
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 39 YR
• Patient Weight: 113