VITAL SYNC REMOTE MONITORING SYSTEM 10116080

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-02-07 for VITAL SYNC REMOTE MONITORING SYSTEM 10116080 manufactured by Avnet Inc.

Event Text Entries

[182768101] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[182768102] According to the reporter, the unit did not sound an alarm for "filterline disconnected" or "sensor disconnected" upon initialization. There was no allegation of patient death or serious injury associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2936999-2020-00103
MDR Report Key9683717
Report SourceUSER FACILITY
Date Received2020-02-07
Date of Report2020-02-07
Date of Event2020-01-24
Date Mfgr Received2020-01-25
Date Added to Maude2020-02-07
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 ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1AVNET INC
Manufacturer Street2740 AMERICAN BLVD W, STE 150
Manufacturer CityBLOOMINGTON MN 55431
Manufacturer CountryUS
Manufacturer Postal Code55431
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVITAL SYNC REMOTE MONITORING SYSTEM
Generic NameTRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY
Product CodeDRG
Date Received2020-02-07
Model Number10116080
Catalog Number10116080
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerAVNET INC
Manufacturer Address2740 AMERICAN BLVD W, STE 150 BLOOMINGTON MN 55431 US 55431


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-07

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