MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-05-05 for BROOKSTONE 882101 manufactured by Shenzhen Jinyuan Sports Massager Instrument Co.,lt.
[44507468]
Customer alleges that product caught on fire.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1221298-2016-00002 |
MDR Report Key | 5634183 |
Date Received | 2016-05-05 |
Date of Report | 2016-04-13 |
Date of Event | 2016-01-23 |
Date Facility Aware | 2016-01-25 |
Report Date | 2016-04-13 |
Date Reported to FDA | 2016-04-13 |
Date Added to Maude | 2016-05-05 |
Event Key | 0 |
Report Source Code | Distributor report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BROOKSTONE |
Generic Name | 3D SHIATSU LUMBAR MASSAGER |
Product Code | ISA |
Date Received | 2016-05-05 |
Model Number | 882101 |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SHENZHEN JINYUAN SPORTS MASSAGER INSTRUMENT CO.,LT |
Manufacturer Address | NO 2A BUILDING, SIXTH INDUSTRY GONGMING TOWN, BAOAN DISTRICT SHENZHEN, SHENZHEN GUANGDONG 518106 CH 518106 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-05-05 |