Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVACARE TAYLOR STREET ROLLATOR 9153651315; 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
 

INVACARE TAYLOR STREET ROLLATOR 9153651315; WALKER, MECHANICAL Back to Search Results
Model Number UNKNOWN
Device Problems Detachment Of Device Component (1104); Device Tipped Over (2589)
Patient Problem No Information (3190)
Event Type  malfunction  
Manufacturer Narrative
The left front wheel has fallen off of the rollator.The walker tipped over but the user did not.The futura is the same /similar to all invacare rollators which are, or have been manufactured and/or marketed by invacare in u.S.The alleged incident occurred in (b)(6).
 
Event Description
The left front wheel has fallen off of the rollator.The walker tipped over but the user did not.The futura is the same /similar to all invacare rollators which are, or have been manufactured and/or marketed by invacare in u.S.The alleged incident occurred in (b)(6).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ROLLATOR 9153651315
Type of Device
WALKER, MECHANICAL
Manufacturer (Section D)
INVACARE TAYLOR STREET
1200 taylor street
elyria OH 44036
Manufacturer (Section G)
INVACARE TAYLOR STREET
1200 taylor street
elyria OH 44036
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44035
8003336900
MDR Report Key5694248
MDR Text Key46372909
Report Number1525712-2016-01839
Device Sequence Number1
Product Code ITJ
Combination Product (y/n)N
Reporter Country CodeSW
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 05/31/2016
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 NumberUNKNOWN
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 05/31/2016
Initial Date FDA Received06/02/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
-
-