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

MAUDE Adverse Event Report: JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD MECHANICAL WALKER, ROLLATOR; 890.3825

  • 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
 

JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD MECHANICAL WALKER, ROLLATOR; 890.3825 Back to Search Results
Model Number 6795
Device Problem Crack (1135)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  No Answer Provided  
Event Description
Per dealer, the u shaped connector brack on the bottom of the seat has fallen out.End user alleges the hardware was loose.End user also stated that the seat has now starting cracking s/n (b)(4).Also the right side caster is not swiveling, having issues when the chair is hard to push.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MECHANICAL WALKER, ROLLATOR
Type of Device
890.3825
Manufacturer (Section D)
JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD
yunyang industrial park
danyang city
jiangsu pro
CH 
MDR Report Key4205483
MDR Text Key4961791
Report Number1531186-2014-05133
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 Manufacturer
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 10/28/2014,10/06/2014
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 Number6795
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA10/28/2014
Distributor Facility Aware Date10/06/2014
Device Age21 MO
Date Report to Manufacturer10/28/2014
Initial Date Manufacturer Received Not provided
Initial Date FDA Received10/28/2014
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-