MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-04-10 for PACEART OPTIMA PAOPT17SUP manufactured by Medtronic, Inc..
[105260444]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[105260445]
It was reported that the clinician imported atrial lead measurements retrieved from the programmer; however, the atrial lead measurements were stored in the ventricular lead measurement fields in the patient management database application. The clinician had to manually edit the fields to change the measurements from the ventricular field to the atrial fields. The issue was escalated to technical services. The application remains in use. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2182208-2018-00620 |
MDR Report Key | 7419653 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2018-04-10 |
Date of Report | 2018-04-10 |
Date of Event | 2018-01-03 |
Date Mfgr Received | 2018-01-03 |
Date Added to Maude | 2018-04-10 |
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 | ANNE SCHILLING |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635052036 |
Manufacturer G1 | MEDTRONIC, INC. |
Manufacturer Street | 8200 CORAL SEA STREET NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal Code | 55112 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PACEART OPTIMA |
Generic Name | ANALYZER, PACEMAKER GENERATOR FUNCTION, INDIRECT |
Product Code | KRE |
Date Received | 2018-04-10 |
Model Number | PAOPT17SUP |
Catalog Number | PAOPT17SUP |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC, INC. |
Manufacturer Address | 8200 CORAL SEA STREET NE MOUNDS VIEW MN 55112 US 55112 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-04-10 |