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

MAUDE Adverse Event Report: DANYANG MAXTHAI MEDICAL EQUIPMENT ECONOMY ROLLATOR W/HAND BRAKE W/CURVE BKRST 9153644547; WALKER, MECHANICAL

  • 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
 

DANYANG MAXTHAI MEDICAL EQUIPMENT ECONOMY ROLLATOR W/HAND BRAKE W/CURVE BKRST 9153644547; WALKER, MECHANICAL Back to Search Results
Model Number 65650
Device Problem Bolus mechanism failure (1067)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
The dealer reported that the frame bar underneath the basket was broken on the 65650 rollator in question.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ECONOMY ROLLATOR W/HAND BRAKE W/CURVE BKRST 9153644547
Type of Device
WALKER, MECHANICAL
Manufacturer (Section D)
DANYANG MAXTHAI MEDICAL EQUIPMENT
danyang
CH 
MDR Report Key4429226
MDR Text Key15113385
Report Number1531186-2015-00362
Device Sequence Number1
Product Code ITJ
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 01/16/2015,01/07/2015
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 Number65650
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA01/16/2015
Distributor Facility Aware Date01/07/2015
Device Age8 MO
Date Report to Manufacturer01/16/2015
Initial Date Manufacturer Received Not provided
Initial Date FDA Received01/16/2015
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-