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

MAUDE Adverse Event Report: INVACARE CLEVELAND STREET INVACARE MATRX PERSONAL BACK10 PLUS 20 IN WIDE TALL HT.; CUSHION, WHEELCHAIR

  • 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 CLEVELAND STREET INVACARE MATRX PERSONAL BACK10 PLUS 20 IN WIDE TALL HT.; CUSHION, WHEELCHAIR Back to Search Results
Model Number PPR20
Device Problems Break (1069); Detachment Of Device Component (1104)
Patient Problem No Information (3190)
Event Type  malfunction  
Manufacturer Narrative
Should additional information become available a supplemental record will be filed.
 
Event Description
Dealer is stating that the he has a ppr20 at the pine valley nursing facility that the lower mounting pins have snapped off on both sides.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
INVACARE MATRX PERSONAL BACK10 PLUS 20 IN WIDE TALL HT.
Type of Device
CUSHION, WHEELCHAIR
Manufacturer (Section D)
INVACARE CLEVELAND STREET
899 cleveland street
elyria OH 44036
Manufacturer (Section G)
INVACARE CLEVELAND STREET
899 cleveland street
elyria OH 44036
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44035
8003336900
MDR Report Key5379123
MDR Text Key36346550
Report Number1219590-2016-00008
Device Sequence Number1
Product Code IMP
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 01/04/2016
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 NumberPPR20
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 01/04/2016
Initial Date FDA Received01/20/2016
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
-
-