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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVAMEX MECHANICAL (MANUAL) WHEELCHAIR; 890.3850

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INVAMEX MECHANICAL (MANUAL) WHEELCHAIR; 890.3850 Back to Search Results
Model Number TREX26R
Device Problems Crack (1135); Material Separation (1562)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 08/14/2014
Event Type  malfunction  
Event Description
It was reported by the dealer that the back is cracking and separating in the middle of the back.No patient injury reported, no additional information provided.
 
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Brand Name
MECHANICAL (MANUAL) WHEELCHAIR
Type of Device
890.3850
Manufacturer (Section D)
INVAMEX
parque industrial manimex
reynosa 8878 0
MX  88780
Manufacturer (Section G)
INVAMEX
parque industrial manimex
reynosa 8878 0
MX   88780
Manufacturer Contact
karen loughren
one invacare way
elyria, OH 44035
8003336900
MDR Report Key4068647
MDR Text Key4851524
Report Number9616091-2014-01793
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 08/14/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/08/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberTREX26R
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received08/14/2014
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;
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