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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVACARE CANADA KIRKLAND MECHANICAL (MANUAL) WHEELCHAIR; 890.3850

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INVACARE CANADA KIRKLAND MECHANICAL (MANUAL) WHEELCHAIR; 890.3850 Back to Search Results
Model Number MYON
Device Problem Device Inoperable (1663)
Patient Problem No Information (3190)
Event Type  malfunction  
Event Description
Brake extensions are breaking off the wheel locks.
 
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Brand Name
MECHANICAL (MANUAL) WHEELCHAIR
Type of Device
890.3850
Manufacturer (Section D)
INVACARE CANADA KIRKLAND
16769 hymus blvd.
kirkland qc H9H 3L4
CA  H9H 3L4
Manufacturer (Section G)
INVACARE CANADA KIRKLAND
16769 hymus blvd.
kirkland qc H9H 3L4
CA   H9H 3L4
Manufacturer Contact
karen loughren
one invacare way
elyria, OH 44035
8003336900
MDR Report Key4112764
MDR Text Key17694761
Report Number3002416487-2014-00094
Device Sequence Number1
Product Code IOR
Combination Product (y/n)N
Reporter Country CodeCA
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 09/03/2014
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 NumberMYON
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 09/03/2014
Initial Date FDA Received09/24/2014
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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