STRAIGHT SUCTION 9733449 EM ENT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-26 for STRAIGHT SUCTION 9733449 EM ENT manufactured by Medtronic Navigation, Inc.

Event Text Entries

[185082895] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[185082896] Medtronic received information regarding instruments used with a navigation system. It was reported that the site had five bent instruments. All five were tested and they were all found with visible damage on a few of them. They were unable to verify without serious manipulation in the divot. There was no patient present.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1723170-2020-01071
MDR Report Key9883605
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-03-06
Date Mfgr Received2020-03-06
Device Manufacturer Date2015-12-01
Date Added to Maude2020-03-26
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 ContactSTACY RUEMPING
Manufacturer Street7000 CENTRAL AVENUE NE RCW215
Manufacturer CityMINNEAPOLIS MN 55432
Manufacturer CountryUS
Manufacturer Postal55432
Manufacturer Phone7635260594
Manufacturer G1MEDTRONIC NAVIGATION, INC
Manufacturer Street826 COAL CREEK CIRCLE
Manufacturer CityLOUISVILLE CO 80027
Manufacturer CountryUS
Manufacturer Postal Code80027
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTRAIGHT SUCTION 9733449 EM ENT
Generic NameINSTRUMENT, STEREOTAXIC
Product CodeHAW
Date Received2020-03-26
Model Number9733449
Catalog Number9733449
Lot Number15120135
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC NAVIGATION, INC
Manufacturer Address826 COAL CREEK CIRCLE LOUISVILLE CO 80027 US 80027


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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