SINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS FD-410LR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2018-05-23 for SINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS FD-410LR manufactured by Olympus Medical Systems Corp..

Event Text Entries

[109119464] The subject device referenced in this report has not yet been returned to olympus for evaluation. Therefore the exact cause of the reported event could not be conclusively determined at this time. A supplemental report will be submitted, if additional or significant information becomes available at a later time.
Patient Sequence No: 1, Text Type: N, H10


[109119465] During an unspecified procedure, the subject device was used. In the procedure, the subject device stopped output and the subject device could not be used. There was bleeding occurred but not bleeding profusely. The intended procedure was completed with another device. There was no patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010047-2018-00926
MDR Report Key7539603
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2018-05-23
Date of Report2018-06-19
Date of Event2018-05-01
Date Mfgr Received2018-05-25
Device Manufacturer Date2017-01-20
Date Added to Maude2018-05-23
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 ContactMR KAZUTAKA MATSUMOTO
Manufacturer Street2951 ISHIKAWA-CHO
Manufacturer CityHACHIOJI-SHI, TOKYO-TO 192-8507
Manufacturer CountryJA
Manufacturer Postal192-8507
Manufacturer Phone426425177
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS
Generic NameSINGLE USE ELECTROSURGICAL HEMOSTATIC FORCEPS
Product CodeKGE
Date Received2018-05-23
Returned To Mfg2018-05-22
Model NumberFD-410LR
Lot NumberK71200
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS MEDICAL SYSTEMS CORP.
Manufacturer Address2951 ISHIKAWA-CHO HACHIOJI-SHI, TOKYO-TO US


Patients

Patient NumberTreatmentOutcomeDate
10 2018-05-23

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