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

MAUDE Adverse Event Report: INVACARE REHABILITATION EQUIP POWERED WHEELCHAIR; 890.3860

  • 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 REHABILITATION EQUIP POWERED WHEELCHAIR; 890.3860 Back to Search Results
Model Number AIRPTMBDY18
Device Problem Charging Problem (2892)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 06/25/2014
Event Type  malfunction  
Event Description
Per provider batteries not holding a charge.Joystick shows batteries are charged, but they aren't.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
POWERED WHEELCHAIR
Type of Device
890.3860
Manufacturer (Section D)
INVACARE REHABILITATION EQUIP
no.435 xieyu street
suzhou industrial park
jiangsu, p.rc. 2150 26
CH  215026
Manufacturer (Section G)
INVACARE REHABILITATION EQUIP
no.435 xieyu street
suzhou industrial park
jiangsu, p.rc. 2150 26
CH   215026
Manufacturer Contact
gregory stevens
one invacare way
elyria, OH 44035
8003336900
MDR Report Key3984529
MDR Text Key18035170
Report Number3008262382-2014-00495
Device Sequence Number1
Product Code ITI
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 06/25/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/06/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberAIRPTMBDY18
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received06/25/2014
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
Patient Outcome(s) Other;
-
-