TA PREMIUM 010470

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2017-09-26 for TA PREMIUM 010470 manufactured by Covidien Lp Llc North Haven.

Event Text Entries

[87316770] Any required fields that are unpopulated are blank because the information is currently unknown or unavailable. A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[87316771] According to the reporter, during a sub total gastrectomy procedure, the surgeon clamped the tissue and started to squeeze the handle, however could not fire the device. The procedure was completed with manual suturing. The status of the patient is no problem.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219930-2017-07389
MDR Report Key6893267
Report SourceFOREIGN,USER FACILITY
Date Received2017-09-26
Date of Report2017-08-30
Date of Event2017-08-30
Date Mfgr Received2017-08-30
Date Added to Maude2017-09-26
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 FDA3
Event Location3
Manufacturer ContactSHARON MURPHY
Manufacturer Street60 MIDDLETOWN AVE
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034925267
Manufacturer G1COVIDIEN LP LLC NORTH HAVEN
Manufacturer Street195 MCDERMOTT RD
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal Code06473
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTA PREMIUM
Generic NameAPPARATUS, SUTURING, STOMACH AND INTESTINAL
Product CodeFHM
Date Received2017-09-26
Model Number010470
Catalog Number010470
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN LP LLC NORTH HAVEN
Manufacturer Address195 MCDERMOTT RD NORTH HAVEN CT 06473 US 06473


Patients

Patient NumberTreatmentOutcomeDate
10 2017-09-26

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