MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2014-01-13 for TENDRIL STS 2088TC/58 SMTFY999 manufactured by St. Jude Medical Inc. Crmd.
[20119185]
It was reported that pt presented in clinic and the right ventricular lead exhibited low lead impedance, high pacing thresholds and a sensing anomaly. It was clinically resolved by a reprogramming and the pt will continue to be monitored.
Patient Sequence No: 1, Text Type: D, B5
[20384801]
All info provided by mfr, no medwatch form was received. This historical complaint is being filed as part of a retrospective review of complaint files in response to a recent fda inspection. There is no change to the actual performance of the product and this report only represents an enhancement to the reporting criteria going forward.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2017865-2014-06386 |
MDR Report Key | 4134759 |
Report Source | 05 |
Date Received | 2014-01-13 |
Date of Event | 2012-09-18 |
Date Facility Aware | 2012-09-18 |
Date Mfgr Received | 2012-09-18 |
Device Manufacturer Date | 2012-05-01 |
Date Added to Maude | 2014-10-07 |
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 | 0 |
Event Location | 3 |
Manufacturer Contact | CARY LAWLER |
Manufacturer Street | 15900 VALLEY VIEW CT. |
Manufacturer City | SYLMAR CA 91342 |
Manufacturer Country | US |
Manufacturer Postal | 91342 |
Manufacturer Phone | 8184932621 |
Manufacturer G1 | ST. JUDE MEDICAL INC. CRMD |
Manufacturer Street | 15900 VALLEY VIEW CT. |
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 | TENDRIL STS |
Generic Name | PERMANENT PACEMAKER ELECTRODE |
Product Code | DTS |
Date Received | 2014-01-13 |
Model Number | 2088TC/58 |
Catalog Number | SMTFY999 |
Device Expiration Date | 2015-05-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 4 MO |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ST. JUDE MEDICAL INC. CRMD |
Manufacturer Address | 15900 VALLEY VIEW CT. SYLMAR CA 91342 US 91342 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-01-13 |