MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2014-01-13 for TENDRIL STS 2088TC/58 SMTFY999 manufactured by St. Jude Medical, Crmd.
[4950614]
It was reported that the pulse generator exhibited high lead impedance and the helix was difficult to retract. The lead was removed and replaced.
Patient Sequence No: 1, Text Type: D, B5
[12374673]
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. Evaluation description: analysis was normal. No anomaly was found.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2017865-2014-07014 |
| MDR Report Key | 4121410 |
| Report Source | 05,06 |
| Date Received | 2014-01-13 |
| Date of Event | 2012-10-08 |
| Date Facility Aware | 2012-10-08 |
| Date Mfgr Received | 2012-10-08 |
| Device Manufacturer Date | 2012-07-01 |
| Date Added to Maude | 2014-10-03 |
| 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 |
| 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 |
| Returned To Mfg | 2012-10-19 |
| Model Number | 2088TC/58 |
| Catalog Number | SMTFY999 |
| Device Expiration Date | 2015-07-31 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | 3 MO |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ST. JUDE MEDICAL, CRMD |
| Manufacturer Address | 15900 VALLEY VIEW CT. SYLMAR CA 91342 US 91342 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-01-13 |