MAUDE Adverse Event Report: D.T. DAVIS ENTERPRISES LTD. HOVERTECH HOVER JACK; LIFT, PATIENT, AC-POWERED

Model Number HJ3902T

Device Problems Overheating of Device (1437); Fumes or Vapors (2529)

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

Event Date 09/15/2022

Event Type  malfunction  

Event Description

Hovertech battery compartment overheated and started emitting fumes.Device was removed from building to prevent odors from reaching patient care area.Batteries were not that old and may have overcharged resulting in overheating and may have caught fire if not caught in time.

• Brand Name: HOVERTECH HOVER JACK
• Type of Device: LIFT, PATIENT, AC-POWERED
• Manufacturer (Section D): D.T. DAVIS ENTERPRISES LTD.
• MDR Report Key: 17020061
• MDR Text Key: 316221892
• Report Number: MW5117960
• Device Sequence Number: 1
• Product Code: FNG
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Biomedical Engineer
• Type of Report: Initial
• Report Date: 05/24/2023

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
• Device Operator: Health Professional
• Device Model Number: HJ3902T
• Device Catalogue Number: CDVC0096446
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 05/26/2023
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1