MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2014-07-22 for TENDRIL STS 2088TC/52 SMTFY999 manufactured by St. Jude Medical, Inc, Crmd.
[4639457]
New information (b)(6) 2014 indicates the lead continues to exhibit noise.
Patient Sequence No: 1, Text Type: D, B5
[4793239]
It was reported that the right ventricular lead exhibited noise with oversensing. The lead remained implanted.
Patient Sequence No: 1, Text Type: D, B5
[12242969]
All information provided by manufacturer, 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 | 2017865-2014-07325 |
MDR Report Key | 3951261 |
Report Source | 05,06,07 |
Date Received | 2014-07-22 |
Date of Event | 2012-08-02 |
Date Facility Aware | 2012-08-02 |
Date Mfgr Received | 2012-08-02 |
Device Manufacturer Date | 2011-04-01 |
Date Added to Maude | 2014-10-06 |
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 COURT |
Manufacturer City | SYLMAR CA 91342 |
Manufacturer Country | US |
Manufacturer Postal | 91342 |
Manufacturer Phone | 8184932621 |
Manufacturer G1 | ST. JUDE MEDICAL, INC |
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, DTS |
Product Code | DTS |
Date Received | 2014-07-22 |
Model Number | 2088TC/52 |
Catalog Number | SMTFY999 |
Device Expiration Date | 2014-04-30 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 15 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 COURT SYLMAR CA 91342 US 91342 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-07-22 |