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

MAUDE Adverse Event Report: INVAMEX TOPAZ 26X20 EXPORT UK; WHEELCHAIR, 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
 

INVAMEX TOPAZ 26X20 EXPORT UK; WHEELCHAIR, MECHANICAL Back to Search Results
Model Number 9TPZ
Device Problem Mechanical Problem (1384)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Manufacturer Narrative
Should additional information become available, a supplemental record will be filed.   mdr is being submitted as a result of a retrospective complaint review.
 
Event Description
The big tire came off the rim and he cannot get it back on.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
TOPAZ 26X20 EXPORT UK
Type of Device
WHEELCHAIR, MECHANICAL
Manufacturer (Section D)
INVAMEX
parque industrial manimex
reynosa 88780
MX  88780
Manufacturer (Section G)
INVAMEX
parque industrial manimex
reynosa 88780
MX   88780
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44035
8003336900
MDR Report Key5758148
MDR Text Key48450129
Report Number9616091-2016-01000
Device Sequence Number1
Product Code IOR
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 08/29/2012
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/29/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number9TPZ
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/04/2012
Is the Reporter a Health Professional? No
Date Manufacturer Received08/29/2012
Was Device Evaluated by Manufacturer? Yes
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
-
-