MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07,company representative, report with the FDA on 2014-10-16 for PLASMABLADE 3.0S PS210-030S manufactured by Medtronic Advanced Energy, Llc.
[5020369]
During a routine preventative maintenance check, the facility's biomed department reported that the unit was found to have high output on coag 6. All other settings were fine. No patient impact.
Patient Sequence No: 1, Text Type: D, B5
[12415630]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[103814269]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1226420-2014-00101 |
MDR Report Key | 4176330 |
Report Source | 05,07,COMPANY REPRESENTATIVE, |
Date Received | 2014-10-16 |
Date of Report | 2014-09-17 |
Date of Event | 2014-09-17 |
Date Mfgr Received | 2014-09-17 |
Date Added to Maude | 2014-10-29 |
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 | KAYLEE BOISVERT |
Manufacturer Street | 180 INTERNATIONAL DRIVE |
Manufacturer City | PORTSMOUTH NH 03801 |
Manufacturer Country | US |
Manufacturer Postal | 03801 |
Manufacturer Phone | 6038426234 |
Manufacturer G1 | MEDTRONIC ADVANCED ENERGY, LLC |
Manufacturer Street | 180 INTERNATIONAL DRIVE |
Manufacturer City | PORTSMOUTH NH 03801 |
Manufacturer Country | US |
Manufacturer Postal Code | 03801 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PLASMABLADE 3.0S |
Generic Name | ELECTROSURGICAL DEVICE |
Product Code | DWG |
Date Received | 2014-10-16 |
Returned To Mfg | 2014-10-10 |
Model Number | PS210-030S |
Catalog Number | PS210-030S |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC ADVANCED ENERGY, LLC |
Manufacturer Address | 180 INTERNATIONAL DRIVE PORTSMOUTH NH 03801 US 03801 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-10-16 |