MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-31 for LIGHT SOURCE, 500XL, XENON 72200568 manufactured by Smith & Nephew, Inc..
[81572218]
(b)(6).
Patient Sequence No: 1, Text Type: N, H10
[81572219]
It was reported that device light started flickering and then blew. After a while wires started to burn or melt, smoke everywhere. No injuries were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1643264-2017-00445 |
MDR Report Key | 6753778 |
Date Received | 2017-07-31 |
Date of Report | 2017-11-10 |
Date of Event | 2017-07-21 |
Date Mfgr Received | 2017-11-07 |
Date Added to Maude | 2017-07-31 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
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 |
Manufacturer Contact | JAMES GONZALES |
Manufacturer Street | 7000 W. WILLIAM CANNON DR |
Manufacturer City | AUSTIN TX 78735 |
Manufacturer Country | US |
Manufacturer Postal | 78735 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 76 S. MERIDIAN AVE. |
Manufacturer City | OKLAHOMA CITY OK 731076512 |
Manufacturer Country | US |
Manufacturer Postal Code | 731076512 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | LIGHT SOURCE, 500XL, XENON |
Generic Name | LIGHT, SURGICAL, FLOOR STANDING |
Product Code | FSS |
Date Received | 2017-07-31 |
Catalog Number | 72200568 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 76 S. MERIDIAN AVE. OKLAHOMA CITY OK 731076512 US 731076512 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-07-31 |