3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV) 3100 A 23689-012

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-24 for 3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV) 3100 A 23689-012 manufactured by Vyaire Medical.

Event Text Entries

[180707492] Any additional information provided by the customer will be included in a follow up report. Technical support will send a technician on site to troubleshoot the suspect device. At this time, the suspect device has not been evaluated. Therefore, no root cause could be determined yet.
Patient Sequence No: 1, Text Type: N, H10


[180707493] The customer reported that there was a problem with the map pressure and loosing pressure on different patients on the 3100 a ventilator. The customer confirmed that there was no patient harm or injury that was associated with the reported event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2021710-2020-11469
MDR Report Key9747441
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-24
Date of Report2020-01-28
Date of Event2020-01-28
Date Mfgr Received2020-01-28
Device Manufacturer Date2012-08-02
Date Added to Maude2020-02-24
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 ContactMINDY FABER
Manufacturer Street26125 N. RIVERWOODS BLVD.
Manufacturer CityMETTAWA, IL
Manufacturer CountryUS
Manufacturer Phone7570116
Manufacturer G1VYAIRE MEDICAL INC.
Manufacturer Street1100 BIRD CENTER DRIVE
Manufacturer CityPALM SPRINGS, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)
Generic NameVENTILATOR, HIGH FREQUENCY
Product CodeLSZ
Date Received2020-02-24
Model Number3100 A
Catalog Number23689-012
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerVYAIRE MEDICAL
Manufacturer Address22745 SAVI RANCH PKWY YORBA LINDA, IL US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-24

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