Brand Name | XPO W/SUPPLEMENTAL BATTERY 9153648167 |
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 Key | 4873339 |
MDR Text Key | 6259540 |
Report Number | 1031452-2015-14515 |
Device Sequence Number | 1 |
Product Code |
CAW
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Distributor,distributor |
Reporter Occupation |
Medical Equipment Company Technician/Representative
|
Type of Report
| Initial |
Report Date |
08/11/2015 |
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 Number | XPO100B |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 08/11/2015 |
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
06/02/2015 |
Initial Date FDA Received | 06/27/2015 |
Was Device Evaluated by Manufacturer? |
Yes
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
|