• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LERADO ZHONGSHAN PEACEFUL COVE BUSINESS TRADING CO DRIVE; POWERED WHEELCHAIR

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

LERADO ZHONGSHAN PEACEFUL COVE BUSINESS TRADING CO DRIVE; POWERED WHEELCHAIR Back to Search Results
Model Number SFPRO417FS-2
Device Problem Break (1069)
Patient Problems Bruise/Contusion (1754); Fall (1848)
Event Date 06/28/2021
Event Type  Injury  
Event Description
(b)(6) is the initial importer of the device which is a power mobility scooter.The device has not been returned for evaluation.In an overabundance of caution we are filing this report.We will submit a followup report if any additional data becomes available.While the customer was crossing the street without using a curb when both wheels and axel came off device from the rear apparatus.She fell in the street,hit her head,and went to the hospital.She did not have any serious injuries, only a stiff neck.She uses the device as an alternative to taking an uber or bus.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
DRIVE
Type of Device
POWERED WHEELCHAIR
Manufacturer (Section D)
LERADO ZHONGSHAN PEACEFUL COVE BUSINESS TRADING CO
no.26, guangfu road,
dong shen
zhong shan, guangdong 52841 4
CH  528414
MDR Report Key12201881
MDR Text Key262617667
Report Number2438477-2021-00029
Device Sequence Number1
Product Code ITI
UDI-Device Identifier00822383991788
UDI-Public822383991788
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Other
Type of Report Initial
Report Date 07/20/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/21/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model NumberSFPRO417FS-2
Distributor Facility Aware Date07/06/2021
Device Age9 MO
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Hospitalization;
Patient Age77 YR
Patient Weight79
-
-