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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVACARE FLORIDA OPERATIONS XPO2 PORTABLE CONCENTRATOR 9153648166; GENERATOR, OXYGEN, PORTABLE

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INVACARE FLORIDA OPERATIONS XPO2 PORTABLE CONCENTRATOR 9153648166; GENERATOR, OXYGEN, PORTABLE Back to Search Results
Model Number XPO100
Device Problems Defective Alarm (1014); Failure to Power Up (1476)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Manufacturer Narrative
(b)(4) 2015 - additional information received per enduser: "all the indicator lights went out on the device.I removed battery and all connections, then put battery back and reconnected and everything worked fine."should additional information become available, a supplemental record will be filed.
 
Event Description
The consumer stated the unit is shutting down with no code.
 
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Brand Name
XPO2 PORTABLE CONCENTRATOR 9153648166
Type of Device
GENERATOR, OXYGEN, PORTABLE
Manufacturer (Section D)
INVACARE FLORIDA OPERATIONS
2101 east lake mary blvd
sanford FL 32773
Manufacturer (Section G)
INVACARE FLORIDA OPERATIONS
2101 east lake mary blvd
sanford FL 32773
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44035
8003336900
MDR Report Key5222389
MDR Text Key31386150
Report Number1031452-2015-16714
Device Sequence Number1
Product Code CAW
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Patient
Type of Report Initial
Report Date 10/21/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/13/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberXPO100
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received10/21/2015
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
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