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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 9TPZ
Device Problem Material Separation (1562)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Event Description
Per customer, the rear wheel has come apart at the seam.
 
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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 Key4126870
MDR Text Key4937059
Report Number9616091-2014-02032
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 09/10/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/29/2014
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? No
Is the Reporter a Health Professional? No
Date Manufacturer Received09/10/2014
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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