Brand Name | KENMORE |
Type of Device | HUMIDIFIER |
Manufacturer (Section D) |
SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTI |
2381 executive center dr. |
boca raton FL 33431 |
|
Manufacturer (Section G) |
CHUZHOU DONLIM ELECTRICAL APPLIANCES CO.,LTD. |
no.1777 yangzi east road |
|
chuzhou, 23900 0 |
CH
239000
|
|
Manufacturer Contact |
michael
miles
|
303 nelson ave. |
neosho, MO 64850
|
4174557441
|
|
MDR Report Key | 6576689 |
MDR Text Key | 75623250 |
Report Number | 3010341502-2017-00119 |
Device Sequence Number | 1 |
Product Code |
KFZ
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
05/18/2017 |
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 |
Other
|
Device Model Number | 31193 |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 05/18/2017 |
Was Device Evaluated by Manufacturer? |
No
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
|
|