MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-19 for SNOWDEN-PENCER PIN 889765 WO144226 manufactured by Carefusion 2200, Inc.
[184079527]
Turned on light to test, worked, when turned off noted burning smell. Unplugged, endo was melted. Did not reach patient. New light and cord obtained, no further issues.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9853221 |
| MDR Report Key | 9853221 |
| Date Received | 2020-03-19 |
| Date of Report | 2020-02-04 |
| Date of Event | 2019-11-08 |
| Report Date | 2020-02-04 |
| Date Reported to FDA | 2020-02-04 |
| Date Reported to Mfgr | 2020-03-19 |
| Date Added to Maude | 2020-03-19 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| 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 | SNOWDEN-PENCER |
| Generic Name | LIGHT, SURGICAL, FLOOR STANDING |
| Product Code | FST |
| Date Received | 2020-03-19 |
| Model Number | PIN 889765 |
| Catalog Number | WO144226 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION 2200, INC |
| Manufacturer Address | 5 SUNNEN DR SAINT LOUIS MO 63143 US 63143 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-19 |