THERMACHOICE TC033

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07 report with the FDA on 2011-12-02 for THERMACHOICE TC033 manufactured by Ethicon, Inc..

Event Text Entries

[16422721] (b)(4). Conclusion: no conclusion can be drawn at this time. Should add'l info be obtained, a supplemental 3500a form will be submitted accordingly. In addition, a review of the batch mfg records was conducted and the batch met all finished goods release criteria.
Patient Sequence No: 1, Text Type: N, H10


[16536478] It was reported that a pt underwent an endometrial thermal ablation procedure on an unk date. During the procedure, the balloon burst when inflated with naci 0. 9%. Add'l info has been requested.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2210968-2011-02047
MDR Report Key2360926
Report Source01,05,06,07
Date Received2011-12-02
Date of Report2011-11-01
Report Date2011-11-01
Date Mfgr Received2011-11-01
Device Manufacturer Date2010-10-01
Date Added to Maude2012-01-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactDANIEL LAMONT
Manufacturer StreetROUTE 22 WEST PO BOX 151
Manufacturer CitySOMERVILLE NJ 088760151
Manufacturer CountryUS
Manufacturer Postal088760151
Manufacturer Phone9082182708
Manufacturer G1ETHICON, INC. - JUAREZ
Manufacturer StreetAVE DE LAS TORRES #7125 COL SALVARCAR
Manufacturer CityJUAREZ, CHIH 32580
Manufacturer CountryMX
Manufacturer Postal Code32580
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameTHERMACHOICE
Generic NameCHATHETER, BALLOON, TRANSCERVICAL
Product CodeMKN
Date Received2011-12-02
Model NumberNA
Catalog NumberTC033
Lot NumberCLMG11
ID NumberNA
Device Expiration Date2012-10-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerETHICON, INC.
Manufacturer AddressSOMERVILLE NJ 08876015 US 08876 0151


Patients

Patient NumberTreatmentOutcomeDate
10 2011-12-02

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