MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-02-24 for SONICISION manufactured by Covidien.
[68232056]
Patient Sequence No: 1, Text Type: N, H10
[68232057]
Device was working but blinking red and stopped working.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6356088 |
| MDR Report Key | 6356088 |
| Date Received | 2017-02-24 |
| Date of Report | 2017-01-23 |
| Date of Event | 2016-12-27 |
| Report Date | 2017-01-23 |
| Date Reported to FDA | 2017-01-23 |
| Date Reported to Mfgr | 2017-01-23 |
| Date Added to Maude | 2017-02-24 |
| 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 |
| 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 | SONICISION |
| Generic Name | STERILIZATION WRAP CONTAINERS, TRAYS, CASSETTES & OTHER ACCESSORIES |
| Product Code | KCT |
| Date Received | 2017-02-24 |
| Operator | PHYSICIAN |
| Device Availability | * |
| Device Age | 1 DY |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Manufacturer Address | 5920 LONGBOW DR. BOULDER CO 80301 US 80301 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-02-24 |