TENDRIL STS 2088TC/58 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/58 SMTFY999 manufactured by St. Jude Medical, Cardiac Rhythm Management Divisi.

Event Text Entries

[19369539] 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


[19557642] It was reported that the right ventricular lead dislodged after implant. The lead was repositioned the same day and remained implanted.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2017865-2014-06609
MDR Report Key4152195
Report Source05,06,07
Date Received2014-01-13
Date of Event2012-10-08
Date Facility Aware2012-10-08
Date Mfgr Received2012-10-08
Date Added to Maude2014-10-09
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, CARDIAC RHYTHM MANAGEMENT DIVISI
Manufacturer Street15900 VALLEY VIEW CT.
Manufacturer CitySYLMAR CA 91342
Manufacturer CountryUS
Manufacturer Postal Code91342
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameTENDRIL STS
Generic NameIMPLANTABLE PACEMAKER ELECTRODE
Product CodeDTS
Date Received2014-01-13
Model Number2088TC/58
Catalog NumberSMTFY999
Device Expiration Date2015-07-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age3 MO
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI
Manufacturer Address15900 VALLEY VIEW CT. SYLMAR CA 91342 US 91342


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2014-01-13

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