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

MAUDE Adverse Event Report: COM-BRIDGE INTERNATIONAL CO. LTD. ENDURANCE QUAD CANE

  • 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
 

COM-BRIDGE INTERNATIONAL CO. LTD. ENDURANCE QUAD CANE Back to Search Results
Model Number ST802-CBL
Device Problem Fracture (1260)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 10/13/2022
Event Type  malfunction  
Event Description
End user was at a truck stop getting coffee when he started to walk with the quad cane and it snapped in two under the curve of the handle.There was no fall or injury.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ENDURANCE QUAD CANE
Type of Device
QUAD CANE
Manufacturer (Section D)
COM-BRIDGE INTERNATIONAL CO. LTD.
unit 1, no. 66, yulong 3 road
dong sheng town
zhong shan city, guangdong, 52841 4
CH  528414
MDR Report Key15808799
MDR Text Key303800261
Report Number1056127-2022-00013
Device Sequence Number1
Product Code IPS
UDI-Device Identifier00754756913206
UDI-Public754756913206
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 11/16/2022,10/19/2022
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 Lay User/Patient
Device Model NumberST802-CBL
Device Catalogue NumberW1302BL
Was Device Available for Evaluation? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA11/16/2022
Distributor Facility Aware Date10/19/2022
Device Age8 MO
Event Location Other
Date Report to Manufacturer11/08/2022
Initial Date Manufacturer Received Not provided
Initial Date FDA Received11/16/2022
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Age62 YR
Patient SexMale
Patient Weight113 KG
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-