TENDRIL STS 2088TC/52 SMTFY999

MAUDE Adverse Event Report

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 2014-01-13 for TENDRIL STS 2088TC/52 SMTFY999 manufactured by St. Jude Medical, Crmd.

Event Text Entries

[4963918] It was reported that during implant the lead exhibited low impedance and insulation anomaly. The lead was explanted.
Patient Sequence No: 1, Text Type: D, B5


[12390509] 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. The reported field event of insulation anomaly was confirmed in laboratory. The damage found was that of a crush that has happened during implant. It has resulted in electrical short which confirm low lead impedance noted in field.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2017865-2014-04617
MDR Report Key4192015
Report Source05,06,07
Date Received2014-01-13
Date of Event2011-05-06
Date Facility Aware2011-05-06
Date Mfgr Received2011-05-19
Device Manufacturer Date2011-03-01
Date Added to Maude2014-10-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location3
Manufacturer ContactCARY LAWLER
Manufacturer Street15900 VALLEY VIEW CT.
Manufacturer CitySYLMAR CA 91342
Manufacturer CountryUS
Manufacturer Postal91342
Manufacturer Phone8184932621
Manufacturer G1ST. JUDE MEDICAL, CRMD
Manufacturer Street15900 VALLEY VIEW CT.
Manufacturer CitySYLMAR CA 91342
Manufacturer CountryUS
Manufacturer Postal Code91342
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTENDRIL STS
Generic NamePERMANENT PACEMAKER ELECTRODE
Product CodeDTS
Date Received2014-01-13
Returned To Mfg2011-05-19
Model Number2088TC/52
Catalog NumberSMTFY999
Device Expiration Date2014-03-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age1 MO
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL, CRMD
Manufacturer Address15900 VALLEY VIEW CT. SYLMAR CA 91342 US 91342


Patients

Patient NumberTreatmentOutcomeDate
10 2014-01-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.