PURSTRING INSTRUMENT 215 020240

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 2020-03-02 for PURSTRING INSTRUMENT 215 020240 manufactured by Covidien Lp Llc North Haven.

Event Text Entries

[184871092] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[184871093] According to the reporter during a roux-en-y gastric bypass, when performing a trial with the device, some of the purse-string suture of the esophagus was unable to be sutured. Additional suture was performed and the procedure was completed. The event occurred during the procedure, but the product was not used for patient. The surgical time was extended by less than 30 min. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219930-2020-00980
MDR Report Key9777689
Report SourceFOREIGN,USER FACILITY
Date Received2020-03-02
Date of Report2020-03-02
Date of Event2020-02-11
Date Mfgr Received2020-02-12
Date Added to Maude2020-03-02
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 ContactLISA HERNANDEZ
Manufacturer Street60 MIDDLETOWN AVE.
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034925563
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 NamePURSTRING INSTRUMENT 215
Product CodeGDJ
Date Received2020-03-02
Model Number020240
Catalog Number020240
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 2020-03-02

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