AUTO ENDO5 ML AE05ML

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-26 for AUTO ENDO5 ML AE05ML manufactured by Teleflex Medical.

Event Text Entries

[137557890] (b)(4). The device has not been returned for investigation. The device history review for the product auto endo5 ml lot# 73j1800032 investigation did not show issues related to the complaint. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[137557891] It was reported that the clips do not open. They got stuck in the tip of the applier.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003898360-2019-00198
MDR Report Key8371147
Date Received2019-02-26
Date of Report2019-02-05
Date of Event2019-01-25
Date Mfgr Received2019-03-25
Device Manufacturer Date2018-09-04
Date Added to Maude2019-02-26
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 ContactJASMINE BROWN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9193614124
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetRANCHO EL DESCANSO
Manufacturer CityTECATE 21478
Manufacturer CountryMX
Manufacturer Postal Code21478
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameAUTO ENDO5 ML
Product CodeGEF
Date Received2019-02-26
Returned To Mfg2019-02-25
Catalog NumberAE05ML
Lot Number73J1800032
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-26

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