MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for ELLIPSE DR CD2411-36Q manufactured by St. Jude Medical, Inc.(crm-sylmar).
[185798656]
The results of the investigation are inconclusive since the device was not returned for analysis. Based on the information received, the cause of the reported incident could not be conclusively determined.
Patient Sequence No: 1, Text Type: N, H10
[185798657]
It was reported that the patient experienced multiple high voltage therapy due to polymorphic ventricular tachycardia and fibrillation. It was noted that the implantable cardioverter defibrillator detected the arrhythmia appropriately but did not sense a few events due to the polymorphic ventricular tachycardia. It was also noted that the device sinus detection was programmed to detect too fast. The rhythm was quickly classified as a sinus rhythm after a high voltage therapy. This caused a delay in therapy because the device had to re-classify the continued arrhythmia. No programming changes were made at this time and the clinic elected to continue to monitor the patient. The patient was reported to be in stable condition.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2017865-2020-04474 |
| MDR Report Key | 9906303 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2020-03-31 |
| Date of Report | 2020-03-31 |
| Date of Event | 2020-03-17 |
| Date Mfgr Received | 2020-03-18 |
| Device Manufacturer Date | 2018-06-29 |
| Date Added to Maude | 2020-03-31 |
| 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 | ELIZABETH BOLTZ |
| Manufacturer Street | 15900 VALLEY VIEW COURT |
| Manufacturer City | SYLMAR CA 91342 |
| Manufacturer Country | US |
| Manufacturer Postal | 91342 |
| Manufacturer G1 | ST. JUDE MEDICAL, INC.(CRM-SYLMAR) |
| Manufacturer Street | 15900 VALLEY VIEW COURT |
| Manufacturer City | SYLMAR CA 91342 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 91342 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ELLIPSE DR |
| Generic Name | IMPLANTABLE CARDIOVERTER DEFIBRILLATOR |
| Product Code | NVZ |
| Date Received | 2020-03-31 |
| Model Number | CD2411-36Q |
| Catalog Number | CD2411-36Q |
| Lot Number | A000060776 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ST. JUDE MEDICAL, INC.(CRM-SYLMAR) |
| Manufacturer Address | 15900 VALLEY VIEW COURT SYLMAR CA 91342 US 91342 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-31 |